CA2012926A1 - Preparation of ascorbic acid 2-phosphate and of 5,6- isopropylideneascorbic acid and potassium magnesium l-ascorbate 2-phosphate as an advantageous salt of l-ascorbic acid 2-phosphate - Google Patents
Preparation of ascorbic acid 2-phosphate and of 5,6- isopropylideneascorbic acid and potassium magnesium l-ascorbate 2-phosphate as an advantageous salt of l-ascorbic acid 2-phosphateInfo
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- CA2012926A1 CA2012926A1 CA002012926A CA2012926A CA2012926A1 CA 2012926 A1 CA2012926 A1 CA 2012926A1 CA 002012926 A CA002012926 A CA 002012926A CA 2012926 A CA2012926 A CA 2012926A CA 2012926 A1 CA2012926 A1 CA 2012926A1
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- Prior art keywords
- ascorbic acid
- phosphate
- until
- kmgpo4
- acetone
- Prior art date
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Abstract
- 28 - O.Z. 0050/40665 Abstract of the Disclosure: Ascorbic acid 2-phosphate is prepared by reacting ascorbic acid or an ascorbic acid derivative with POCl3 in the presence of a tertiary amine in a suitable aqueous solvent at from -10 to 25°C while maintaining a pH of about 8-13.5 with KOH during the entire phosphorylation reaction and then isolating -the ascorbic acid 2-phosphate, by a process in which an aqueous solution of a magnesium compound is added to the reaction mixture obtained in the phosphorylation, without prior treatment with an ion exchanger, until the forma-tion of crystalline KMgPO4 is complete, the KMgPO4 which is crystallized out is separated off, the resulting fil-trate is evaporated down at a pH of from 6 to 11 and/or from 0.1 to 5 times the amount, based on the evaporated filtrate, of a lower primary alkanol or acetone is added and the stirred mixture is cooled until KCl has completely crystallized out, and the ascorbic acid phosphate is iso-lated in a conventional manner from the reaction solution obtained by separating off KCl and substantially freed from inorganic salts. It is particularly advantageous if the ascorbic acid 2-phosphate is isolated in the form of the novel potassium magnesium ascorbate 2-phosphate, which is also claimed.
The process is particularly advantageous if the ascorbic acid derivative used is 5,6-isopropylidene-ascorbic acid which has been obtained by reacting ascor-bic acid with acetone in the presence of oleum. The process is particularly important for the preparation of L-ascorbic acid 2-phosphate.
The process is particularly advantageous if the ascorbic acid derivative used is 5,6-isopropylidene-ascorbic acid which has been obtained by reacting ascor-bic acid with acetone in the presence of oleum. The process is particularly important for the preparation of L-ascorbic acid 2-phosphate.
Description
2 ~ 2 ~
O.Z. 0050/40665 Preparation of ascorbic acid 2-phosphate and of 5 6-1sopropylideneascorbic_acid and potassium maqnesi L-ascorbate 2-phosphate as an advantaqeous salt of L-ascorbic acid 2-~hosphate The present invention relates to a process for the preparation of mono- or diphosphates of ascorbic acid, in particular of L-ascorbic acid, and a particularly advan-tageous method for the preparation of the 5,6-isopropy-lideneascorbic acid required for this purpose. The pre-sent invention furthermore relates to potassium magnesium L-ascorbate 2-phosphate, by means of which L-ascorbic acid 2-phosphate can be particularly advantageously isolated.
L-ascorbic acid lvitamin C) forms a vital p~rt of balanced human nutrition and inclusion of this vitamin in tha diet has been recommended. However, vitamin C is the least stable vitamin in foods since it reacts ~xtxemely easily with atm ipheric oxygen. It is known, for ex-ample, that ascorbic acid reacts rapidly with oxygen to give dehydroascorbic acid, a compound which, although retaining the full vitamin C activity, decomposes rapidly and irreversibly into compounds without vitamin C activ-ity. Ascorbic acid is also decomposed at high tempera-tures by dehydration in an acidic medium. Thus, efforts to incorporate L-ascorbic acid directly into dough or bakery products which are to be subsequently baked have proven ineffective since only small amounts of the vitamin C activity of the L-ascorbic acid withstand cook-ing and baking at high temperatures. Regarding the use of vitamin C in the animal feed sector, it is also very important for the vitamin to be present in a very heat-stable form so that the vitamin loss during incorporation in the animal feed by extrusion and pelletizing is very small. Vitamin C has recently become important in fish farming and shrimp farming. It is known that ascorbic acid can be made more stable to oxygen and heat by con-verting it into suitable derivatives.
201~2~
- 2 - O.Z. 0050/40665 Ascorbic acid monophosphate has the following important advantages over free ascorbic acid:
1) rela~ively high stability to oxidation, 2) general bioavailability since it can be cleaved by phosphatases in vivo and in vitro to give ~scorbic acid (this has been demorlstrated, for example, in guinea pigs, broilers, piglets, Rhesus monkeys and fish), 3) high heat stability and hence the possibility of processing in extruders and 4) high stability to hydrolysis.
The preparation of vitamin C phosphate was first described by Cutolo and Larizza (cf. Gazz. Chim. Ital. 91 (1961), 964). The preparation starts from ascorbic acid or 5,6-isopropylideneascorbic acid, which is phosphory-lated with POCl3 in the presence of pyridine and a strong base in water.
Some modifications to this process were subse~
quently published in the literature, and it was long a matter of contention as to whether the product obtained is ascorbic acid 2-phosphate or 3-phosphate, until this question wa~ clearly answered by Jernow (cf. Tetrahedron, 35 (1979), 1483 et seq.). Some of this work is described in the said publication (loc cit). The most advantageous process to date for the preparation of ascorbic acid 2-phosphate is the process described in German Laid-Open Application DOS 2,719,303.
The disadvantage of all stated processes is that they are suitable only for use on a small scale, since the working up described is much too expensive for an industrial procedure. The problem is that the desired product has to be separated off from a large excess of inorganic salts originating from the phosphorylation process. For example, in the process described in German Laid-Open Application DOS 2,719,303, the phosphorylation gives a reaction solution which contains a~out 4.5 equivalents of KCl and 1.8 equivalents of R3PO4, ie. about -, , ~"
.
2~2~2~
- 3 - ~.Z. ooso/~0665 6 equivalents of organic salts together, per equivalent of de~ired product.
According to German Laid-Open Application DOS
2,719,303, this solution is first passed over an ion exchanger in order to exchange the potassium ions for hydrogen ions. Since the salt concentration (KCl, ~3P04~
potassium isopropylidene-L-ascorbic acid 2-phosphate) is very hiqh, the procedure must be carried out in great dilution so that ion exchange takes place completely. In an industrial process, the resulting large volumes give rise to high capital costs and enormous energy costs for evaporation. In the subsequent neutralization with MgO, a large excess of base is required since, in addition to the acid obtained as the product, it is also necessary to neutralize the total excess HCl and H3PO4. Moreover, it is difficult to separate off Mg3(PO4)z since it is obtained in very finely divided form and is extremely difficult to filter. Furthermore, some of the ascorbic acid phosphate is precipitated with the finely divided Mg3PO4 and is therefore lost.
In this process, the desired product is precipi-tated as an Ng salt with an alcohol, and it is necessary to choose the conditions so that the large amount of MgCl2 which forms from MgO and ~Cl during the neutralization remains in solution. According to our investigationq, it was not possible to obtain an ascorbic acid phosphate free of inorganic salts, in spite of thorough washing of the product with large amounts of aqueous ethanol. In order to obtain a pure product by this process, it was necessary to redissolve the Mg ascorbic acid phosphate, converted into the acidic form using an ion exchanger and to convert th~ product into a recrystalli~able salt usinq an auxiliary base, such as cyclohexylamine. The product purified in this manner was then converted into the desired salt.
Such a process is inconvenient and uneconomical and involves large losses and is therefore unsuitable for industrial production.
;
` 2~2~2~
- ~ - o.z. ooso/4066s It is an object of the present invention to make the working up of the reaction mixture obtained in the phosphorylation of ascorbic acid or ascorbic acid deriva-tives with POC13 in the presence of tertiary amines by the process of German Laid-Open Application DOS 2,719,303 so advantageous that the industrial production of ascor-bic acid phosphate is possible by this method.
- We have found that this object is achieved and that, surprisingly, the free phosphoric acid present in the reaction solution and some of the cations of the solution, which are present as K3PO4 at the pH of the reaction solution of 7 or higher, preferably from 11 to 13, can be removed in a simple manner in the presence of all reaction products (ascorbic acid derivatives, KCl, K3PO4) and auxiliary reagents (tertiary amine, such as pyridine) if a magnesium compound, preferably an aqueous solution of an Mg compound, is added to the reaction solution. Despite the high concentration of salts and solids, the phosphoric acid combines to form a sparingly soluble salt which has the composition KMgPO4 and forms well defined crystals which can readily be filtered off from the reaction solution, while at the same time the pH
decreases to 7-11, preferably 9.0-10.5. The reaction can be carried out at from 0 to 50C, preferably at about 20C. The KMgP04 obtained is very pure and can be used directly as a fertilizer salt. It is particularly advantageous to use magnesium chloride as the magnesium compound since in this case the potassi~ displaced by the magnesium is present as XCl, which is in any case already present in the reaction mixture.
It was very surprising that a sparingly soluble salt which has the composition KMgPO4 is obtained in high purity and can be readily separated off by filtration is formed from a solution containing so many components.
It is a decisive advantage that, as a result of these measures, some of the salt load of the reaction mixture can be separated off in the form of a salt which ;:
, 2~g~
. 5 _ O.Z. OOSO/40665 can be used as a fertilizer, without ~ubstantial amounts of the desired product being copr~cipitated. This per-mits an economical and environmentally compa~ible pro-cess, since the salt load of the wastewaters is greatly reduced in this manner.
Removal of the inorganic phosphate is furthermore a great advantage since, consequently, a smaller amount of ion exchange resin is required for separating off the potassium and subsequently less Mg base is required for neutralization and no poorly fi.lterable Mg3(PO4)z is ob-tained during the neutralization.
The present invention therefore relates to a process for the preparation of ascorbic acid 2-phosphate by reac~ing ascorbic acid or an ascorbic acid derivative which has a group of the formula I
H-C~R I
H--C{}R2 (I) H--C--O`C=O
=I
~30 OH
where Rl and R2 are each hydrogen or together form one of the groups \CH 3 or CH~3 with POC13 in the presence of a tertiary ~mine in a suit-able aqueous solvent at -10 to 25C while maintaining a pH of about 8-13.5, preferably 10-13, by adding KOH
during the entire phosphoryla~ion reaction, and then isolating the a~corbic acid ~-phosphate, wherein, to separate off the excPss inorganic phosphate, about the stoichiometric amount of a magnesium compound, advan-tageously in t:he form of an aqueous solution, is added to the reaction mixture obtained in the phosphorylation, .
.
g ~ ~
- 6 - O.Z. 0050/~0665 directly and without prior ion exchange treatment, at a pH > 7, until the formation of crystallin~ KMgPo4 is complete, the KMgPo4 which has crystallized out is sepa-rated off and the ascorbic acid phosphate is isolated from the filtrate in a conventional manner.
The phosphorylation is advantageously carried out under the conditions describ~ed in German Laid-Open Application DOS 2,719,303.
In addition to ascorbic acid, suitable ascorbic acid derivatives which contain a group of the formula I
H--C--O--R I
H-C~R2 (I) H--C--O`C=O
C=C
~) OH
where Rl and R2 are each hydrogen or together form one of the groups or ~CH~
are the alkali metal salts or alkaline earth metal salts of ascorbic acid and its salts with a base-stable protec-~ive group at the carbon atom in the 6-position, for example 5,6-O-isopropylideneascorbic acid and 5,6-O-benzylideneascorbic acid. These compounds can be used in the four differen~ stereoisomeric forms. The process is particularly important for the reaction of L-ascorbic acid and its derivatives.
Suitabie tertiary amines are those which are mis-cible with the reaction mixture and are nonvolatile and have an ionization constant of less ~han about 107.
Examples are lower trialkylamines, such as triethylamine, and cyclic amines, such as pyridine and ~ or ~-picoline.
, 2 ~ 2 g _ 7 _ o.z. 0050/40665 The best yields are obtained using pyridine.
About 5 moles of the amine are used pe~: mole of ascorbic acid.
The phosphorylation takes place particularly S advantageously if the concentration of the amine in the reaction mixture is about 1.5-3, preferably 2.2-2.6, moles and that of the ascorbic acid is about 0.3-0.6, preferably 0.4-0.5, mole per liter.
An advantageously used sol~ent is water.
In general, the reaction temperature used should be the lowest temperature at w~hich the reaction mixture remains liquid and at which the tertiary amine does not form a separate phase. Temperatures of from -10 to +10C
are suitable.
Examples of suitable magnesium compounds are MgBr2 and MgSO4, and in particular magnesium chloride. It is advantageous to add the magnesium salt in the form of an aqueous solution.
The amount of magnesium salt is in general about 90-110 mol ~, based on inorganic phosphate present in the rea~tion mixture.
The novel process is very advantageous if A) the starting material used is an ascorbic acid derivative which has a group of the formula I where R1 and R2 are each hydrogen or together form one of the groups \C\ ~r \CH~
B) an aqueou~ solution of a magnesium compound, prefer-ably magnesium chloride, is ~dded to the reaction mixture obtained in the phosphorylation, without prior treatment with an ion exchanger, until the formation of crystalline RMgP04 iS complete, C) the KMgP04 which is crystallized out is separated off, `
2~12~2~
- 8 - O.Z. 0050/40665 D) to separate off the inorganic potassium salts the resulting filtrate is ev~porated to a solids content of from 20 to 90, preferably from 40 to 50, % by weight at a pH of from 6 to 11, preferably from 7.5 to 8, and cooled to a temperature of from -10 to +20C until the potassium salts or potassium chloride have or has completely crystallized out, or the filtrate obtained after KMgP04 has crystal-lized out and been separated off is evaporated down at a pH of from 6 to 11, preferably from 7.5 to 8, and from 0.1 to 5, preferably from 0.8 to 1.2, times the amount, based on the filtrate used, of a lower primary alkanol or acetone is then added at from 0 to 60C, preferably from 20 to 30C, and the stirred mixture is cooled to a temperature of from -20 to 20C, preferably from 0 to 10C, until the potassilm salts or KCl have or has completely crystallized out, and E) the ascorbic acid phosphate is isolated in a conven-tional manner from the reaction solution which is obtained by separati~g off the potassium salts or KCl and substantially freed from inorganic salts.
For further details of this isolation, reference may be made to, for example, German ~aid-Open ~pplication DOS 2,719,303.
The reaction mixture is advantageously brought to the suitable pH by adding KOH solution or HCl solution.
The tertiary ~mine, in particular pyridine, can readily be separa~ed off and recovered from the conden-sate obtained in the evaporation in step E, and can be reused for the phosphorylation.
Examples of lower primary alkanols are the water-soluble alkanols of 1 to 4 carbon atoms, in par~icular methanol.
The alkanol is added in general at from 0 to 60C, preferably from 20 to 30C, and stirring and removal of the KCl is effected at from -20 to 50C, preferably .
2~1292~
_ 9 _ O.Z. ()050/~0665 from 0 to 10C. The crystals are washed with alcohol or alcohol/water mixture and are then very pure and can be used for other purposes.
It is surprising that the isopropylideneascorbic S acid phosphate, which is present as the potassium, dipotas-sium or tripotassium salt, remains completely in solution, especially when it is considered that the basic alkali metal and alkaline earth metal c;alts of ascorbic acid 2-phosphate are precipitated by the addition of alcohols.
It is a decisive advantage -that a further part of the salt load can be saparated off in the form of the useful salt. This is economical and environmentally com-patible since the salt load of the wastewaters is reduced as a result. If the precipitated potassium salt is to be further used, and if it has to be a pure salt, magnesium chloride must be used as the magnesium compound.
Another considerable advantage is that a smaller amount of ion exchange resin is required for converting the potassium isopropylideneascorbic acid 2-phosphate into the acid form and no excess mineral acid is liberated during the ion exchange process.
Consequently, less Mg base is required for the neutralization too. A further advantage is that any base can be used in this procedure for neutralizing the ion exchange eluate which i free of mineral acid, since, in the subsequent crystallization, there is no longer any danger that inorganic salts will be precipitated together with the desired product. This is particularly advanta-geous if the cyclohexylammonium salt is to be prepared for subsequent ultrapurification, since this salt can then be prepared directly from the ion e~change eluate with the result that crystallization by the magnesium salt is superfluous.
The novel procesCl is particularly advantageous if the starting material used is an ascorbic acid derivative which has a group of the formula I where Rl and R2 together form the group :
2~292~
- 10 - ~). Z . O0S0/~0665 C
C ~ 3 and which was prepared by treatment, for from 1 to 8, preferably from S to 6, hour.s at from -20 to +40C, preferably from -10 to ~10C, with a mixture obtained by adding from 0to 65, preferably about 20 to 30, ~strength by weight oleum to acetone containing from 0 to 5, prefer-ably from 0.6 to 1.5, % by weight of water at from -30 to +40C, preferably from -10 to 0C, while stirring, separa-ting off the crystallized 5,6-isopropylideneascorbic acid at about -l5~C and pressinq the crystals dry.
If the phosphorylation is carried out immediately afterward, the product which i9 crystallized out can be pressed dry ~ithout being washed and can be introduced, directly with the residual moisture present, into the aqueous KOH solution.
During the solution process, care should be taken to exclude oxygen.
The amount of oleum is chosen so that the sul-furic acid in the reaction mixture after the reaction i5 about 100-60, pre~erably about 80, ~ s~rength, based on the water content, the amount of w~ter to be bound being calculated from ~he water content of the solvent and from the water formed in the reaction.
A stoichiometric amount of sodium hydroxide solu-tion ~preferably 40-50% strength) corresponding to the amount of acid is added, at from -20 to ~40C, preferably from -10 to +10C, to the mother liquor of the crystals, which liquor now contains acetone, sulfuric acid and traces of ascorbic acid derivatives, Na2SO4.nH2O (n = 3-5) being preci.pitated as a crystalline compound, which can be separated off by filtration. The acetone freed from the crystals can be distilled in good yield to give acetone which has a water content of about 1.4~ and can be reused for the reaction described above. It is a considerable advantage that, using oleum as a catalyst, `
~12~
- ll - O.Z. ~050/40665 acetone having a water content of up to 5% can be used and a conversion of > 99~ still achieved. Oleum is very cheap.
rt is a great advantage that -the catalyst acid can be separated off completely in solid form as Na2SO"
after the reaction and hence acetone can be recovered from the mother liquor in h.igh yield and high purity by filtration and simple distillation.
Because the 5,6-isopropylideneascorbic acid can be used directly in the phosphoxylation, without washing, maximum yields are achieved.
It was very surprising that the reaction to give isopropylideneascorbic acid takes place in the manner described, without detectable formation of byproducts, lS although a large amount of sulfuric acid is present in the reaction mixture.
The result is a particularly advantageous overall process for the preparation of ascorbic acid 2-phosphate, in particular of L-ascorbic acid 2-phosphate, wherein A) ascorbic acid, in particular L-ascorbic acid, is treated, at from -10 to +10C for from 5 to 6 hours, with a mixture obtained by adding from 0 to 65~
strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40C, while stirring, and the 5,6-isopropylidene-L-ascorbic acid which crystallizes out is separated off at about -15C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 to 13.5 by means of KOH and in the presence of a tertiary amine at from -10 to +25C in a suitable aqueous solvent, B) the aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgP04 iS
complete, C) the KMgPO4 which is crystallized out is separated off, 20~926 - 12 - O. Z . 0050/40665 D) to separate off potassium chloride, the resulting filtrate is evaporated down at a pH of from 6 to 11, preferably from 7.5 to 8, and/or from 0.1 to 5, preferably from 0.8 to 1.2, times ~he amount, based on the evaporated filtrate, of a lower alkanol or acetone i5 added and the mixture is cooled to 0-10C
until KCl has co. letely cr~stallized out, and E) the ascorbic acid phosphate or L-ascorbic acid phos-phate is isolated in a conventional manner from the resulting reaction solution substantially freed from inorganic salts.
If the 5,6-isopropylideneascorbic acid prepared by reacting ascorbic acid (derivativesl and acetone in the presence of oleum is not to be further processed immediately but is to be dried and stored, the crystals must be washed repeatedly with ice cold acetone.
The present invention furthermore relates to a process for the preparation of 5,6-isopropylide~eascorbic acid, wherein ascorbic acid is treated, at from -20 to +40C, preferably from -10 to +10C, for from 1 to 8, preferably from 5 to 6, hours, with a mixture obtained by adding from 0 to 65, preferably from 20 to 30, % strength by weight oleum to acetone containing from 0 to 5, preferably from 0.6 to 1.4, ~ by weight of water at from -30 to +40C, preferably from -10 to +10C, while stir ring, and the 5,6-isopropylideneascorbic acid which crystallize3 out is separated off at about -15C, if necessary, after washing with ice-cooled acetone.
The novel process is very particularly advan-tageous if the resulting ascorbic acid 2-phosphate is isolated via a potassium magnesium salt which has not yet been described. Potassium magnesium ascorbate 2-phosphate has very advantageous properties. It is precipitated from solutions in the form of well defined crystals and there-fore has extremely good filtration properties and does not tend to agglomerate on drying~ It has a defined con-tent of water of crystallization and is not hygroscopic.
2~292~
- 13 - O.Z. 0050/4n665 Since, in contrast to the pure magnesium salt, it con-tains only 3 instead of 5 moles of water of crystalliza-tion per mole of ascorbate, the vitamin C content of such a dry powder is higher. A purer product, ie. one which has been freed from bis-(2,2'-ascorbate) phosphate, is obtained on precipitating the ascorbic acid 2-phosphate as a calcium salt. However, the yields achievable here by crystallization are about 20~ lower.
The present invention therefore also relates to the novel advantageous potassi~ magnesium ascorbate 2-phosphate. In this mixed salt, potassium and magnesium need not be present in an exactly stoichiometric ratio.
The potassium/magnesium ratio in the solution from which the mixed salt is precipitated is identical to that of the crystalline product obtained therefrom. Optimum results are obtained in the isolation of ascorbic acid 2-phosphate in the form of a potassium/magnesium mixed salt if the salt has a composition of about Klt03Mg~0 15 ascor-bate 2-phosphate. The byproduct bis-(2,2'-ascorbate) phosphate crystallizes out in the X/Mg mixed salt in the same ratio as in the pure magnesium salt.
To isolatetheascorbic acid2-phosphate intheform of the X/Mg mixed salt, in general the aqueo~s reaction solution which is obtained after ~he inorganic potassium salts have been separated off and which has been substan-tiallyfreedfrominorganicsaltsispassedoveramoderat~ly acidic cation exchanger, if necessary after removal of the lower alkanol or acetone used for precipitating KCl, and dilution with water, and MgO, Mg(OH)2 or MgCO3 is intro-duced into the resulting acidic eluate with cooling untilthe pH has increased to 7. The reaction solution obtained i5 then stirred for about 4 to 10, preferably 5 to 7, hours, stirred to remove suspended particles, evaporated down in a rotary evaporator and finally stirred into excess lower alkanol,preferablymethanol,oracetone.ThisgiYesindivi-dual crystals which can readily be filtered. These crys-tals can easily be dried under nitrogen in a drying oven.
, .
.
:. . ~
~0~29~
- 1~ - O.Z. 0050/40665 The pre~ent invention accordingly also relates to the process, described above, for the preparation of L-ascorbic acid 2-phosphate in the form of potassi~lm magnesium L-ascorbate 2-phosphate, wherein S A) L-ascorbic acid is treated, at from -10 to +10C for from 5 to 6 hours, with a Mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to ~40C while stirrinc;, the 5,6-isopropylidene-L-ascorbic acid which crystallizes out i5 separated off at about -15C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 to 13.5 by means of KOH and in the presence of a tertiary amine at from -10 to +25C in a suitable aqueous solvent, B) an aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phospho.ryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline RMgP04 iS
complete, C) the KMgPO4 which is crystallized out is separated off, D) to separate off potassium chloride the resulting filtrate is evapora~ed down at a pH of from 6 to 11 and/or from 0.1 to 5, preferably from 0.8 to 1.2, times the amountr based on the filtrate which may have been evaporated down, of a lower alkanol or acetone is added and the mixture i5 cooled to 0-10C
until KCl has completely crystallized out, E) ~he resulting reaction solution which has been sub-stantially freed from inorganic salts is treated with a moderately acidic cation exchanger which loses its exchange capacity at a pH of from about 2.0 to 0.5, preferably from 1.2 to 0.8, and F) the L-ascorbic acid 2-phosphate is precipitated in the form of the novel potassium magnesium ascorbate 2-phosphate from the resulting reaction mixture essentially containing the monopotassium salt of L-, -~0~2926 - 15 - o.Z. 0050/40665 ascorbic acid 2-phosphate, by adding MgO, Mg(OH)2 or MgCO3 until the solution has a pH of about 7 and if necessary treating the solution with methanol or acetone.
5Moderately acidic cation exchangers which lose their exchange capacity at a p~ of from about 2.0 to 0.5 are understood as being essentially gel-like or macro-porous exchange resins which consist of a copolymer of styrene and divinylbenzene and carry suitable covalently 10bonded functional groups.
Particularly suitable functional groups are the following groups:
~CH ~ , in which a) R1 = H and R2 = -CH 2-P~
b) R1 = R2 - -CH 2-ll/
OH
15C ) Rl = R2 = -CH2-~:OOH
or d) R1 = H and R2 = -CH2-COOH
In addition to the special resins, it is also possible to U52 other resins if they have a similar composition, ie. if they carry the stated ~unctional 20groups or functional groups having the same action. In comparison, exchange resins which carry only -COOH groups are not sufficiently acidic and tho-~e which carry -SO3H
groups are too acidic.
Examples are Lewatit OC1060 and Lewatit TP 207 and TP 208.
Lewati~ OC 1060, which no longer has a mea~urable exchange capacity at a pH of about 0.5 i5 particularly suitable. This ensures that only 2 of the 3 ~ ions in the potassium salt of the ascorbic acid 2-phosphate are exchanged. This is a particular advantage if it is intended to prepare po~assium magnesium L-ascorbate 2-phosphate, since in this way R' is removed only in an amount which is subsequently to be replaced by Mg2+.
-: ~
2Q~2~2~
- 16 - o.Z. 0050/4066s rn this reaction procedure, the reaction time for eliminating the isopropylidene protective group is about 2 hours at 30C.
The great advantage of the use of moderately acidic ion exchangers compared with the use of strongly acidic ion exchangers in known processes is that the eluate formed is less acidic and the ascorbic acid 2-phosphate therefore does not undergo cleavage to form ascorbic acid again, which has a very advantageous effect on the product quality, in particular the color of the product. Further advantages of the procedure using the novel potassium magnesium L-ascorbate 2-phosphate are:
a) smaller consumption of MgO
b) lower salt emission c) better space-time yield because regeneration times for the ion exchanger are reduced by 1/3.
Neutralization of the resulting eluate with MgO, (OH)2 or MgCO3 is carried out in general at from 20 to 25C. To precipitate the potassium magnesium ascorbate 2-phosphate, the reaction solution is generally evaporated down and then advantageously poured into a lower alkanol or acetone, preferably into methanol.
With the aid of the novel process, it is possible to prepare the desired ascorbic acid ~-phosphates, in particular L-ascorbic acid 2-phospate, as such or in the form of its salts, in particular the novel potassium magnesium aqcorbate 2-phosphate and 5,6-isopropylidene-ascorbic acid which can be used as an in~ermediate, industrially in a very advantageous manner.
A. Preparation of 5,6-isopropylidene-L-ascorbic acid 43 g of 24% strength oleum were added dropwise to 480 ml of acetone (water content about 0.4%). 120 g of L-ascorbic acid were introduced into the resulting mixture at 0C, and the reaction mixture was stirred for 6 hours (h~ at 0C. It was then cooled to -15C and the crystals were filtered off under suction. The resulting 20~9~
- L7 - O.Z. 0050/40665 fllter cake was pressed dry and then further processed as described in B.
The yield was from 97 to 98% of theory, and the content of llnconverted L-ascorblc acid was <0.5%.
S s. Phosp~orylation of 5,6-i.sopropylidene-L-ascorbic acid The filter cake which was obtained according to A and pressed dry was slowly introduced into a mixture of 12n0 ml of water and 300 ml of pyridine, the pH being kept at 12-13 by continuously adding KOH solution.
Thereafter, 146 g of POCl3 were slowly added to the mixture at 0C, the pH being kept at 13 by adding KOH. Stirring was then continued for a further 30 minutes (min) and the reaction mixture was tes+ed for starting material.
C. Precipitation of KMgPO4 .6HzO
70 g of MgCl2.6H2O in the form of an approximately 30~ strength by weight aqueous solution were added to the reaction mixture obtained in ~, and stirring was then carried out for a further hour. The crystalline precipi-tate form~d was then filtered off under suction and the precipitate was washed with twice 100 ml of water and dried. 90 g of KMgPO4.6H20 were obtained in this manner.
D. Precipitation of KCl ~he filtrate obtained in C was evaporated down to 1000 ml, after which 1 l of methanol wa~ added. Stirring was then carried out for 1 h, after which the precipitate formed was filtered off under suction, washed twice with 200 ml of 60 : 40 methanol/water and dried. About 235 g of KCl were obtained.
E. Isolation of L-ascorbic acid phosphate as the magnesium salt The combined filtrates from D were evaporated to about 800 g under reduced pressure and then passed over a column filled with a strongly acidic ion exchanger (Lewatit S-100 in the H+ form). Elution was then carried out using about 1 l of water, and about 2,200 ml of the . .
.
2~29~' - 18 - O.Z. ~050/~066s acidic eluat~ were collected. About 39 g of MgO w~re added to the acidic eluate and the mixture was stirred until virtually everything had dissolved. The pH of the solution was about 8.5-9. A small amount of undissolved material was then filtered off, and the filtrate was evaporated to about 500 g. The solution thus obtained was added dropwise to about 1200 g of methanol, while stirring. The crystals formecl were filtered off under suction, washed with 300 ml of methanol, pressed dry and dried. 210 g of magnesium L~ascorbate 2-phosphate.5H20 were obtained in this manner. The product contained about 7% of 2,2'-bisascorbic acid monophosphate and had a vitamin C contnet of about 46~.
The yield was 80~ of theory, based on vitamin C
used.
The procedure described in Example lA, B and C
was followed. To precipitate KCl, the filtrate obtained according to lC was evaporated to about 600 ml and then stirred for 1 h at 0C. The precipitate formed was then filtered off under suction, washed twice with 200 ml of ice water and dried. About 185 g of RCl were obtained.
To isolate the L-ascorbic acid 2-phosphate as a magnesium salt, the combined filtrates were passed over a strongly acidic ion exchanger (Lewatit S-100 in the H~
form). Elution was then carried out with 1.5 liters of water, and about 2700 ml of the acidic eluate were collec-ted. The eluate was brought to a pH of 9 with MgO. The small amount of undissolved material was then filtered off, and the solution was evaporated to about 600 ml.
Thi~ solution was then added dropwise to 1200 ml of methanol. The crystals formed were filtered off under suction and washed with 5 times 500 ml of a mixture of 1 : 1 methanol/water and once with 300 ml of methanol.
190 q of magnesium L-ascorbate 2-phosphate were obtained in this manner. The resulting product contained about 3% of 2,2'-bis-L-ascorbic acid monophosphate and 2~:1292~
- 19 - O.Z. 0050/40665 had a vitamin C content of about 42~.
Preparation of 5,6-isopropylidene-L-ascorbic acid 55 g of 24~ strength oleum were added dropwise S to 480 ml of acetone (water content about 1.4%) at -10C.
120 g of L-ascorbic acid were introduced into the result-ing mixture at about 0C, and the reaction mixture was stirred for 6 h at 0C. It was then cooled to -15C and the crystals formed were filtered off under suction. The resulting filter cake was pressed dry, washed wi~h twice 100 ml of ice cold acetone and dried at room temperature under reduced pressure from a water pump.
The yield was 97~ of theory.
The procedure described in Example lA, lB, lC and lD was followed.
To isolate ascorbic acid 2-phosphate in the form of the novel potassium magnesium ascorbate 2-phosphate, the combined filtrates from lD were evaporated to about 800 g under reduced pressure, diluted with 200 ml of water and then passed over a column filled with the moderately - acidic ion exchanger Lewatit OC-1060 (polymeric amido~
phosphonic acid, H~ form).
The eluate obtained had a pH of about 1O2. To eliminate the isopropylidene protective group, the eluate was kept at 30C for 2 h and then neutralized with MgO at from 20 to 25C, stirred for a further 6 h, filtered and then evaporated to about 450 g in a rotary evaporator at 80C and thereafter immediately poured into 1100 ml of methanol. The salt which crystallized out was filtered off, washed with methanol and dried.
220 g of individual corn-yellow crystals were obtained, corresponding to a yield of 87.7% of theory, based on ascorbic acid.
Analysis of the salt gave an atomic ratio of Xo~8Mgl~o6c56Hl2spl~ corresponding to the compound KMgC6H6PO9-3~2o .
.- ~ . . , 2~1292~
- 20 - O.Z. 0050/40665 According to HPLC analysis, the product contained 89.0% of ascorbate 2-phosphate and 9.9~ of bis-(2,2'-ascorbate) phosphate.
S To demonstrate the advantageous properties of the novel potassium magnesium L-ascorbate 2-phosphate com-pared with potassium L-ascorbate 2-phosphate and mag-nesium L-ascorbate 2-phosphate, the filtration resis-tance, the agglomeration on drying and the dust formation of potassium magnesium L-ascorbate 2-phosphates of the formula KrMgyC~H6POg~3H2O, ie. of potassium magnesium L-ascorbate 2-phosphates ha~ing different K/Mg ratio~, were compared with the corresponding properties of the potas-sium salts (x = 3, y = 0) or magnesium salts (x = 0, y =
1.5).
Experi- X Y Filtration Agglomeration Dust ment resistance on dryinq formation a) 0.00 1.50 +++ +++ +++
b) 0.08 1.46 +++ +++ +++
c) 0.17 1.~2 +++ ++ ++
d) 0.27 1.37 ++ ++ ++
e) 0.36 1.32 ++ + ++
f) 0.48 1.26 ~ + +
g) 0.61 1.20 - - +
h) 0.75 1.12 - - +
i) 0.83 1.09 - - +
j) 1.08 0.96 - - +
k) 1.20 0.86 - - +
l~ 1.54 0.73 + +
m) 1.86 Q.57 + +
n) 2.15 0.43 + ++
o) 3.00 0.00 Product obtained a~ an oil .
2~29~
- 21 - O.Z. 0050/~0665 The experiments showed that salts having the composition K1~03Mg1~0 lS ascorbate 2 phosphate have the best product properties.
Evaluation scale:
+++ Very great ++ Great + Average - Low
O.Z. 0050/40665 Preparation of ascorbic acid 2-phosphate and of 5 6-1sopropylideneascorbic_acid and potassium maqnesi L-ascorbate 2-phosphate as an advantaqeous salt of L-ascorbic acid 2-~hosphate The present invention relates to a process for the preparation of mono- or diphosphates of ascorbic acid, in particular of L-ascorbic acid, and a particularly advan-tageous method for the preparation of the 5,6-isopropy-lideneascorbic acid required for this purpose. The pre-sent invention furthermore relates to potassium magnesium L-ascorbate 2-phosphate, by means of which L-ascorbic acid 2-phosphate can be particularly advantageously isolated.
L-ascorbic acid lvitamin C) forms a vital p~rt of balanced human nutrition and inclusion of this vitamin in tha diet has been recommended. However, vitamin C is the least stable vitamin in foods since it reacts ~xtxemely easily with atm ipheric oxygen. It is known, for ex-ample, that ascorbic acid reacts rapidly with oxygen to give dehydroascorbic acid, a compound which, although retaining the full vitamin C activity, decomposes rapidly and irreversibly into compounds without vitamin C activ-ity. Ascorbic acid is also decomposed at high tempera-tures by dehydration in an acidic medium. Thus, efforts to incorporate L-ascorbic acid directly into dough or bakery products which are to be subsequently baked have proven ineffective since only small amounts of the vitamin C activity of the L-ascorbic acid withstand cook-ing and baking at high temperatures. Regarding the use of vitamin C in the animal feed sector, it is also very important for the vitamin to be present in a very heat-stable form so that the vitamin loss during incorporation in the animal feed by extrusion and pelletizing is very small. Vitamin C has recently become important in fish farming and shrimp farming. It is known that ascorbic acid can be made more stable to oxygen and heat by con-verting it into suitable derivatives.
201~2~
- 2 - O.Z. 0050/40665 Ascorbic acid monophosphate has the following important advantages over free ascorbic acid:
1) rela~ively high stability to oxidation, 2) general bioavailability since it can be cleaved by phosphatases in vivo and in vitro to give ~scorbic acid (this has been demorlstrated, for example, in guinea pigs, broilers, piglets, Rhesus monkeys and fish), 3) high heat stability and hence the possibility of processing in extruders and 4) high stability to hydrolysis.
The preparation of vitamin C phosphate was first described by Cutolo and Larizza (cf. Gazz. Chim. Ital. 91 (1961), 964). The preparation starts from ascorbic acid or 5,6-isopropylideneascorbic acid, which is phosphory-lated with POCl3 in the presence of pyridine and a strong base in water.
Some modifications to this process were subse~
quently published in the literature, and it was long a matter of contention as to whether the product obtained is ascorbic acid 2-phosphate or 3-phosphate, until this question wa~ clearly answered by Jernow (cf. Tetrahedron, 35 (1979), 1483 et seq.). Some of this work is described in the said publication (loc cit). The most advantageous process to date for the preparation of ascorbic acid 2-phosphate is the process described in German Laid-Open Application DOS 2,719,303.
The disadvantage of all stated processes is that they are suitable only for use on a small scale, since the working up described is much too expensive for an industrial procedure. The problem is that the desired product has to be separated off from a large excess of inorganic salts originating from the phosphorylation process. For example, in the process described in German Laid-Open Application DOS 2,719,303, the phosphorylation gives a reaction solution which contains a~out 4.5 equivalents of KCl and 1.8 equivalents of R3PO4, ie. about -, , ~"
.
2~2~2~
- 3 - ~.Z. ooso/~0665 6 equivalents of organic salts together, per equivalent of de~ired product.
According to German Laid-Open Application DOS
2,719,303, this solution is first passed over an ion exchanger in order to exchange the potassium ions for hydrogen ions. Since the salt concentration (KCl, ~3P04~
potassium isopropylidene-L-ascorbic acid 2-phosphate) is very hiqh, the procedure must be carried out in great dilution so that ion exchange takes place completely. In an industrial process, the resulting large volumes give rise to high capital costs and enormous energy costs for evaporation. In the subsequent neutralization with MgO, a large excess of base is required since, in addition to the acid obtained as the product, it is also necessary to neutralize the total excess HCl and H3PO4. Moreover, it is difficult to separate off Mg3(PO4)z since it is obtained in very finely divided form and is extremely difficult to filter. Furthermore, some of the ascorbic acid phosphate is precipitated with the finely divided Mg3PO4 and is therefore lost.
In this process, the desired product is precipi-tated as an Ng salt with an alcohol, and it is necessary to choose the conditions so that the large amount of MgCl2 which forms from MgO and ~Cl during the neutralization remains in solution. According to our investigationq, it was not possible to obtain an ascorbic acid phosphate free of inorganic salts, in spite of thorough washing of the product with large amounts of aqueous ethanol. In order to obtain a pure product by this process, it was necessary to redissolve the Mg ascorbic acid phosphate, converted into the acidic form using an ion exchanger and to convert th~ product into a recrystalli~able salt usinq an auxiliary base, such as cyclohexylamine. The product purified in this manner was then converted into the desired salt.
Such a process is inconvenient and uneconomical and involves large losses and is therefore unsuitable for industrial production.
;
` 2~2~2~
- ~ - o.z. ooso/4066s It is an object of the present invention to make the working up of the reaction mixture obtained in the phosphorylation of ascorbic acid or ascorbic acid deriva-tives with POC13 in the presence of tertiary amines by the process of German Laid-Open Application DOS 2,719,303 so advantageous that the industrial production of ascor-bic acid phosphate is possible by this method.
- We have found that this object is achieved and that, surprisingly, the free phosphoric acid present in the reaction solution and some of the cations of the solution, which are present as K3PO4 at the pH of the reaction solution of 7 or higher, preferably from 11 to 13, can be removed in a simple manner in the presence of all reaction products (ascorbic acid derivatives, KCl, K3PO4) and auxiliary reagents (tertiary amine, such as pyridine) if a magnesium compound, preferably an aqueous solution of an Mg compound, is added to the reaction solution. Despite the high concentration of salts and solids, the phosphoric acid combines to form a sparingly soluble salt which has the composition KMgPO4 and forms well defined crystals which can readily be filtered off from the reaction solution, while at the same time the pH
decreases to 7-11, preferably 9.0-10.5. The reaction can be carried out at from 0 to 50C, preferably at about 20C. The KMgP04 obtained is very pure and can be used directly as a fertilizer salt. It is particularly advantageous to use magnesium chloride as the magnesium compound since in this case the potassi~ displaced by the magnesium is present as XCl, which is in any case already present in the reaction mixture.
It was very surprising that a sparingly soluble salt which has the composition KMgPO4 is obtained in high purity and can be readily separated off by filtration is formed from a solution containing so many components.
It is a decisive advantage that, as a result of these measures, some of the salt load of the reaction mixture can be separated off in the form of a salt which ;:
, 2~g~
. 5 _ O.Z. OOSO/40665 can be used as a fertilizer, without ~ubstantial amounts of the desired product being copr~cipitated. This per-mits an economical and environmentally compa~ible pro-cess, since the salt load of the wastewaters is greatly reduced in this manner.
Removal of the inorganic phosphate is furthermore a great advantage since, consequently, a smaller amount of ion exchange resin is required for separating off the potassium and subsequently less Mg base is required for neutralization and no poorly fi.lterable Mg3(PO4)z is ob-tained during the neutralization.
The present invention therefore relates to a process for the preparation of ascorbic acid 2-phosphate by reac~ing ascorbic acid or an ascorbic acid derivative which has a group of the formula I
H-C~R I
H--C{}R2 (I) H--C--O`C=O
=I
~30 OH
where Rl and R2 are each hydrogen or together form one of the groups \CH 3 or CH~3 with POC13 in the presence of a tertiary ~mine in a suit-able aqueous solvent at -10 to 25C while maintaining a pH of about 8-13.5, preferably 10-13, by adding KOH
during the entire phosphoryla~ion reaction, and then isolating the a~corbic acid ~-phosphate, wherein, to separate off the excPss inorganic phosphate, about the stoichiometric amount of a magnesium compound, advan-tageously in t:he form of an aqueous solution, is added to the reaction mixture obtained in the phosphorylation, .
.
g ~ ~
- 6 - O.Z. 0050/~0665 directly and without prior ion exchange treatment, at a pH > 7, until the formation of crystallin~ KMgPo4 is complete, the KMgPo4 which has crystallized out is sepa-rated off and the ascorbic acid phosphate is isolated from the filtrate in a conventional manner.
The phosphorylation is advantageously carried out under the conditions describ~ed in German Laid-Open Application DOS 2,719,303.
In addition to ascorbic acid, suitable ascorbic acid derivatives which contain a group of the formula I
H--C--O--R I
H-C~R2 (I) H--C--O`C=O
C=C
~) OH
where Rl and R2 are each hydrogen or together form one of the groups or ~CH~
are the alkali metal salts or alkaline earth metal salts of ascorbic acid and its salts with a base-stable protec-~ive group at the carbon atom in the 6-position, for example 5,6-O-isopropylideneascorbic acid and 5,6-O-benzylideneascorbic acid. These compounds can be used in the four differen~ stereoisomeric forms. The process is particularly important for the reaction of L-ascorbic acid and its derivatives.
Suitabie tertiary amines are those which are mis-cible with the reaction mixture and are nonvolatile and have an ionization constant of less ~han about 107.
Examples are lower trialkylamines, such as triethylamine, and cyclic amines, such as pyridine and ~ or ~-picoline.
, 2 ~ 2 g _ 7 _ o.z. 0050/40665 The best yields are obtained using pyridine.
About 5 moles of the amine are used pe~: mole of ascorbic acid.
The phosphorylation takes place particularly S advantageously if the concentration of the amine in the reaction mixture is about 1.5-3, preferably 2.2-2.6, moles and that of the ascorbic acid is about 0.3-0.6, preferably 0.4-0.5, mole per liter.
An advantageously used sol~ent is water.
In general, the reaction temperature used should be the lowest temperature at w~hich the reaction mixture remains liquid and at which the tertiary amine does not form a separate phase. Temperatures of from -10 to +10C
are suitable.
Examples of suitable magnesium compounds are MgBr2 and MgSO4, and in particular magnesium chloride. It is advantageous to add the magnesium salt in the form of an aqueous solution.
The amount of magnesium salt is in general about 90-110 mol ~, based on inorganic phosphate present in the rea~tion mixture.
The novel process is very advantageous if A) the starting material used is an ascorbic acid derivative which has a group of the formula I where R1 and R2 are each hydrogen or together form one of the groups \C\ ~r \CH~
B) an aqueou~ solution of a magnesium compound, prefer-ably magnesium chloride, is ~dded to the reaction mixture obtained in the phosphorylation, without prior treatment with an ion exchanger, until the formation of crystalline RMgP04 iS complete, C) the KMgP04 which is crystallized out is separated off, `
2~12~2~
- 8 - O.Z. 0050/40665 D) to separate off the inorganic potassium salts the resulting filtrate is ev~porated to a solids content of from 20 to 90, preferably from 40 to 50, % by weight at a pH of from 6 to 11, preferably from 7.5 to 8, and cooled to a temperature of from -10 to +20C until the potassium salts or potassium chloride have or has completely crystallized out, or the filtrate obtained after KMgP04 has crystal-lized out and been separated off is evaporated down at a pH of from 6 to 11, preferably from 7.5 to 8, and from 0.1 to 5, preferably from 0.8 to 1.2, times the amount, based on the filtrate used, of a lower primary alkanol or acetone is then added at from 0 to 60C, preferably from 20 to 30C, and the stirred mixture is cooled to a temperature of from -20 to 20C, preferably from 0 to 10C, until the potassilm salts or KCl have or has completely crystallized out, and E) the ascorbic acid phosphate is isolated in a conven-tional manner from the reaction solution which is obtained by separati~g off the potassium salts or KCl and substantially freed from inorganic salts.
For further details of this isolation, reference may be made to, for example, German ~aid-Open ~pplication DOS 2,719,303.
The reaction mixture is advantageously brought to the suitable pH by adding KOH solution or HCl solution.
The tertiary ~mine, in particular pyridine, can readily be separa~ed off and recovered from the conden-sate obtained in the evaporation in step E, and can be reused for the phosphorylation.
Examples of lower primary alkanols are the water-soluble alkanols of 1 to 4 carbon atoms, in par~icular methanol.
The alkanol is added in general at from 0 to 60C, preferably from 20 to 30C, and stirring and removal of the KCl is effected at from -20 to 50C, preferably .
2~1292~
_ 9 _ O.Z. ()050/~0665 from 0 to 10C. The crystals are washed with alcohol or alcohol/water mixture and are then very pure and can be used for other purposes.
It is surprising that the isopropylideneascorbic S acid phosphate, which is present as the potassium, dipotas-sium or tripotassium salt, remains completely in solution, especially when it is considered that the basic alkali metal and alkaline earth metal c;alts of ascorbic acid 2-phosphate are precipitated by the addition of alcohols.
It is a decisive advantage -that a further part of the salt load can be saparated off in the form of the useful salt. This is economical and environmentally com-patible since the salt load of the wastewaters is reduced as a result. If the precipitated potassium salt is to be further used, and if it has to be a pure salt, magnesium chloride must be used as the magnesium compound.
Another considerable advantage is that a smaller amount of ion exchange resin is required for converting the potassium isopropylideneascorbic acid 2-phosphate into the acid form and no excess mineral acid is liberated during the ion exchange process.
Consequently, less Mg base is required for the neutralization too. A further advantage is that any base can be used in this procedure for neutralizing the ion exchange eluate which i free of mineral acid, since, in the subsequent crystallization, there is no longer any danger that inorganic salts will be precipitated together with the desired product. This is particularly advanta-geous if the cyclohexylammonium salt is to be prepared for subsequent ultrapurification, since this salt can then be prepared directly from the ion e~change eluate with the result that crystallization by the magnesium salt is superfluous.
The novel procesCl is particularly advantageous if the starting material used is an ascorbic acid derivative which has a group of the formula I where Rl and R2 together form the group :
2~292~
- 10 - ~). Z . O0S0/~0665 C
C ~ 3 and which was prepared by treatment, for from 1 to 8, preferably from S to 6, hour.s at from -20 to +40C, preferably from -10 to ~10C, with a mixture obtained by adding from 0to 65, preferably about 20 to 30, ~strength by weight oleum to acetone containing from 0 to 5, prefer-ably from 0.6 to 1.5, % by weight of water at from -30 to +40C, preferably from -10 to 0C, while stirring, separa-ting off the crystallized 5,6-isopropylideneascorbic acid at about -l5~C and pressinq the crystals dry.
If the phosphorylation is carried out immediately afterward, the product which i9 crystallized out can be pressed dry ~ithout being washed and can be introduced, directly with the residual moisture present, into the aqueous KOH solution.
During the solution process, care should be taken to exclude oxygen.
The amount of oleum is chosen so that the sul-furic acid in the reaction mixture after the reaction i5 about 100-60, pre~erably about 80, ~ s~rength, based on the water content, the amount of w~ter to be bound being calculated from ~he water content of the solvent and from the water formed in the reaction.
A stoichiometric amount of sodium hydroxide solu-tion ~preferably 40-50% strength) corresponding to the amount of acid is added, at from -20 to ~40C, preferably from -10 to +10C, to the mother liquor of the crystals, which liquor now contains acetone, sulfuric acid and traces of ascorbic acid derivatives, Na2SO4.nH2O (n = 3-5) being preci.pitated as a crystalline compound, which can be separated off by filtration. The acetone freed from the crystals can be distilled in good yield to give acetone which has a water content of about 1.4~ and can be reused for the reaction described above. It is a considerable advantage that, using oleum as a catalyst, `
~12~
- ll - O.Z. ~050/40665 acetone having a water content of up to 5% can be used and a conversion of > 99~ still achieved. Oleum is very cheap.
rt is a great advantage that -the catalyst acid can be separated off completely in solid form as Na2SO"
after the reaction and hence acetone can be recovered from the mother liquor in h.igh yield and high purity by filtration and simple distillation.
Because the 5,6-isopropylideneascorbic acid can be used directly in the phosphoxylation, without washing, maximum yields are achieved.
It was very surprising that the reaction to give isopropylideneascorbic acid takes place in the manner described, without detectable formation of byproducts, lS although a large amount of sulfuric acid is present in the reaction mixture.
The result is a particularly advantageous overall process for the preparation of ascorbic acid 2-phosphate, in particular of L-ascorbic acid 2-phosphate, wherein A) ascorbic acid, in particular L-ascorbic acid, is treated, at from -10 to +10C for from 5 to 6 hours, with a mixture obtained by adding from 0 to 65~
strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40C, while stirring, and the 5,6-isopropylidene-L-ascorbic acid which crystallizes out is separated off at about -15C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 to 13.5 by means of KOH and in the presence of a tertiary amine at from -10 to +25C in a suitable aqueous solvent, B) the aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgP04 iS
complete, C) the KMgPO4 which is crystallized out is separated off, 20~926 - 12 - O. Z . 0050/40665 D) to separate off potassium chloride, the resulting filtrate is evaporated down at a pH of from 6 to 11, preferably from 7.5 to 8, and/or from 0.1 to 5, preferably from 0.8 to 1.2, times ~he amount, based on the evaporated filtrate, of a lower alkanol or acetone i5 added and the mixture is cooled to 0-10C
until KCl has co. letely cr~stallized out, and E) the ascorbic acid phosphate or L-ascorbic acid phos-phate is isolated in a conventional manner from the resulting reaction solution substantially freed from inorganic salts.
If the 5,6-isopropylideneascorbic acid prepared by reacting ascorbic acid (derivativesl and acetone in the presence of oleum is not to be further processed immediately but is to be dried and stored, the crystals must be washed repeatedly with ice cold acetone.
The present invention furthermore relates to a process for the preparation of 5,6-isopropylide~eascorbic acid, wherein ascorbic acid is treated, at from -20 to +40C, preferably from -10 to +10C, for from 1 to 8, preferably from 5 to 6, hours, with a mixture obtained by adding from 0 to 65, preferably from 20 to 30, % strength by weight oleum to acetone containing from 0 to 5, preferably from 0.6 to 1.4, ~ by weight of water at from -30 to +40C, preferably from -10 to +10C, while stir ring, and the 5,6-isopropylideneascorbic acid which crystallize3 out is separated off at about -15C, if necessary, after washing with ice-cooled acetone.
The novel process is very particularly advan-tageous if the resulting ascorbic acid 2-phosphate is isolated via a potassium magnesium salt which has not yet been described. Potassium magnesium ascorbate 2-phosphate has very advantageous properties. It is precipitated from solutions in the form of well defined crystals and there-fore has extremely good filtration properties and does not tend to agglomerate on drying~ It has a defined con-tent of water of crystallization and is not hygroscopic.
2~292~
- 13 - O.Z. 0050/4n665 Since, in contrast to the pure magnesium salt, it con-tains only 3 instead of 5 moles of water of crystalliza-tion per mole of ascorbate, the vitamin C content of such a dry powder is higher. A purer product, ie. one which has been freed from bis-(2,2'-ascorbate) phosphate, is obtained on precipitating the ascorbic acid 2-phosphate as a calcium salt. However, the yields achievable here by crystallization are about 20~ lower.
The present invention therefore also relates to the novel advantageous potassi~ magnesium ascorbate 2-phosphate. In this mixed salt, potassium and magnesium need not be present in an exactly stoichiometric ratio.
The potassium/magnesium ratio in the solution from which the mixed salt is precipitated is identical to that of the crystalline product obtained therefrom. Optimum results are obtained in the isolation of ascorbic acid 2-phosphate in the form of a potassium/magnesium mixed salt if the salt has a composition of about Klt03Mg~0 15 ascor-bate 2-phosphate. The byproduct bis-(2,2'-ascorbate) phosphate crystallizes out in the X/Mg mixed salt in the same ratio as in the pure magnesium salt.
To isolatetheascorbic acid2-phosphate intheform of the X/Mg mixed salt, in general the aqueo~s reaction solution which is obtained after ~he inorganic potassium salts have been separated off and which has been substan-tiallyfreedfrominorganicsaltsispassedoveramoderat~ly acidic cation exchanger, if necessary after removal of the lower alkanol or acetone used for precipitating KCl, and dilution with water, and MgO, Mg(OH)2 or MgCO3 is intro-duced into the resulting acidic eluate with cooling untilthe pH has increased to 7. The reaction solution obtained i5 then stirred for about 4 to 10, preferably 5 to 7, hours, stirred to remove suspended particles, evaporated down in a rotary evaporator and finally stirred into excess lower alkanol,preferablymethanol,oracetone.ThisgiYesindivi-dual crystals which can readily be filtered. These crys-tals can easily be dried under nitrogen in a drying oven.
, .
.
:. . ~
~0~29~
- 1~ - O.Z. 0050/40665 The pre~ent invention accordingly also relates to the process, described above, for the preparation of L-ascorbic acid 2-phosphate in the form of potassi~lm magnesium L-ascorbate 2-phosphate, wherein S A) L-ascorbic acid is treated, at from -10 to +10C for from 5 to 6 hours, with a Mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to ~40C while stirrinc;, the 5,6-isopropylidene-L-ascorbic acid which crystallizes out i5 separated off at about -15C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 to 13.5 by means of KOH and in the presence of a tertiary amine at from -10 to +25C in a suitable aqueous solvent, B) an aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phospho.ryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline RMgP04 iS
complete, C) the KMgPO4 which is crystallized out is separated off, D) to separate off potassium chloride the resulting filtrate is evapora~ed down at a pH of from 6 to 11 and/or from 0.1 to 5, preferably from 0.8 to 1.2, times the amountr based on the filtrate which may have been evaporated down, of a lower alkanol or acetone is added and the mixture i5 cooled to 0-10C
until KCl has completely crystallized out, E) ~he resulting reaction solution which has been sub-stantially freed from inorganic salts is treated with a moderately acidic cation exchanger which loses its exchange capacity at a pH of from about 2.0 to 0.5, preferably from 1.2 to 0.8, and F) the L-ascorbic acid 2-phosphate is precipitated in the form of the novel potassium magnesium ascorbate 2-phosphate from the resulting reaction mixture essentially containing the monopotassium salt of L-, -~0~2926 - 15 - o.Z. 0050/40665 ascorbic acid 2-phosphate, by adding MgO, Mg(OH)2 or MgCO3 until the solution has a pH of about 7 and if necessary treating the solution with methanol or acetone.
5Moderately acidic cation exchangers which lose their exchange capacity at a p~ of from about 2.0 to 0.5 are understood as being essentially gel-like or macro-porous exchange resins which consist of a copolymer of styrene and divinylbenzene and carry suitable covalently 10bonded functional groups.
Particularly suitable functional groups are the following groups:
~CH ~ , in which a) R1 = H and R2 = -CH 2-P~
b) R1 = R2 - -CH 2-ll/
OH
15C ) Rl = R2 = -CH2-~:OOH
or d) R1 = H and R2 = -CH2-COOH
In addition to the special resins, it is also possible to U52 other resins if they have a similar composition, ie. if they carry the stated ~unctional 20groups or functional groups having the same action. In comparison, exchange resins which carry only -COOH groups are not sufficiently acidic and tho-~e which carry -SO3H
groups are too acidic.
Examples are Lewatit OC1060 and Lewatit TP 207 and TP 208.
Lewati~ OC 1060, which no longer has a mea~urable exchange capacity at a pH of about 0.5 i5 particularly suitable. This ensures that only 2 of the 3 ~ ions in the potassium salt of the ascorbic acid 2-phosphate are exchanged. This is a particular advantage if it is intended to prepare po~assium magnesium L-ascorbate 2-phosphate, since in this way R' is removed only in an amount which is subsequently to be replaced by Mg2+.
-: ~
2Q~2~2~
- 16 - o.Z. 0050/4066s rn this reaction procedure, the reaction time for eliminating the isopropylidene protective group is about 2 hours at 30C.
The great advantage of the use of moderately acidic ion exchangers compared with the use of strongly acidic ion exchangers in known processes is that the eluate formed is less acidic and the ascorbic acid 2-phosphate therefore does not undergo cleavage to form ascorbic acid again, which has a very advantageous effect on the product quality, in particular the color of the product. Further advantages of the procedure using the novel potassium magnesium L-ascorbate 2-phosphate are:
a) smaller consumption of MgO
b) lower salt emission c) better space-time yield because regeneration times for the ion exchanger are reduced by 1/3.
Neutralization of the resulting eluate with MgO, (OH)2 or MgCO3 is carried out in general at from 20 to 25C. To precipitate the potassium magnesium ascorbate 2-phosphate, the reaction solution is generally evaporated down and then advantageously poured into a lower alkanol or acetone, preferably into methanol.
With the aid of the novel process, it is possible to prepare the desired ascorbic acid ~-phosphates, in particular L-ascorbic acid 2-phospate, as such or in the form of its salts, in particular the novel potassium magnesium aqcorbate 2-phosphate and 5,6-isopropylidene-ascorbic acid which can be used as an in~ermediate, industrially in a very advantageous manner.
A. Preparation of 5,6-isopropylidene-L-ascorbic acid 43 g of 24% strength oleum were added dropwise to 480 ml of acetone (water content about 0.4%). 120 g of L-ascorbic acid were introduced into the resulting mixture at 0C, and the reaction mixture was stirred for 6 hours (h~ at 0C. It was then cooled to -15C and the crystals were filtered off under suction. The resulting 20~9~
- L7 - O.Z. 0050/40665 fllter cake was pressed dry and then further processed as described in B.
The yield was from 97 to 98% of theory, and the content of llnconverted L-ascorblc acid was <0.5%.
S s. Phosp~orylation of 5,6-i.sopropylidene-L-ascorbic acid The filter cake which was obtained according to A and pressed dry was slowly introduced into a mixture of 12n0 ml of water and 300 ml of pyridine, the pH being kept at 12-13 by continuously adding KOH solution.
Thereafter, 146 g of POCl3 were slowly added to the mixture at 0C, the pH being kept at 13 by adding KOH. Stirring was then continued for a further 30 minutes (min) and the reaction mixture was tes+ed for starting material.
C. Precipitation of KMgPO4 .6HzO
70 g of MgCl2.6H2O in the form of an approximately 30~ strength by weight aqueous solution were added to the reaction mixture obtained in ~, and stirring was then carried out for a further hour. The crystalline precipi-tate form~d was then filtered off under suction and the precipitate was washed with twice 100 ml of water and dried. 90 g of KMgPO4.6H20 were obtained in this manner.
D. Precipitation of KCl ~he filtrate obtained in C was evaporated down to 1000 ml, after which 1 l of methanol wa~ added. Stirring was then carried out for 1 h, after which the precipitate formed was filtered off under suction, washed twice with 200 ml of 60 : 40 methanol/water and dried. About 235 g of KCl were obtained.
E. Isolation of L-ascorbic acid phosphate as the magnesium salt The combined filtrates from D were evaporated to about 800 g under reduced pressure and then passed over a column filled with a strongly acidic ion exchanger (Lewatit S-100 in the H+ form). Elution was then carried out using about 1 l of water, and about 2,200 ml of the . .
.
2~29~' - 18 - O.Z. ~050/~066s acidic eluat~ were collected. About 39 g of MgO w~re added to the acidic eluate and the mixture was stirred until virtually everything had dissolved. The pH of the solution was about 8.5-9. A small amount of undissolved material was then filtered off, and the filtrate was evaporated to about 500 g. The solution thus obtained was added dropwise to about 1200 g of methanol, while stirring. The crystals formecl were filtered off under suction, washed with 300 ml of methanol, pressed dry and dried. 210 g of magnesium L~ascorbate 2-phosphate.5H20 were obtained in this manner. The product contained about 7% of 2,2'-bisascorbic acid monophosphate and had a vitamin C contnet of about 46~.
The yield was 80~ of theory, based on vitamin C
used.
The procedure described in Example lA, B and C
was followed. To precipitate KCl, the filtrate obtained according to lC was evaporated to about 600 ml and then stirred for 1 h at 0C. The precipitate formed was then filtered off under suction, washed twice with 200 ml of ice water and dried. About 185 g of RCl were obtained.
To isolate the L-ascorbic acid 2-phosphate as a magnesium salt, the combined filtrates were passed over a strongly acidic ion exchanger (Lewatit S-100 in the H~
form). Elution was then carried out with 1.5 liters of water, and about 2700 ml of the acidic eluate were collec-ted. The eluate was brought to a pH of 9 with MgO. The small amount of undissolved material was then filtered off, and the solution was evaporated to about 600 ml.
Thi~ solution was then added dropwise to 1200 ml of methanol. The crystals formed were filtered off under suction and washed with 5 times 500 ml of a mixture of 1 : 1 methanol/water and once with 300 ml of methanol.
190 q of magnesium L-ascorbate 2-phosphate were obtained in this manner. The resulting product contained about 3% of 2,2'-bis-L-ascorbic acid monophosphate and 2~:1292~
- 19 - O.Z. 0050/40665 had a vitamin C content of about 42~.
Preparation of 5,6-isopropylidene-L-ascorbic acid 55 g of 24~ strength oleum were added dropwise S to 480 ml of acetone (water content about 1.4%) at -10C.
120 g of L-ascorbic acid were introduced into the result-ing mixture at about 0C, and the reaction mixture was stirred for 6 h at 0C. It was then cooled to -15C and the crystals formed were filtered off under suction. The resulting filter cake was pressed dry, washed wi~h twice 100 ml of ice cold acetone and dried at room temperature under reduced pressure from a water pump.
The yield was 97~ of theory.
The procedure described in Example lA, lB, lC and lD was followed.
To isolate ascorbic acid 2-phosphate in the form of the novel potassium magnesium ascorbate 2-phosphate, the combined filtrates from lD were evaporated to about 800 g under reduced pressure, diluted with 200 ml of water and then passed over a column filled with the moderately - acidic ion exchanger Lewatit OC-1060 (polymeric amido~
phosphonic acid, H~ form).
The eluate obtained had a pH of about 1O2. To eliminate the isopropylidene protective group, the eluate was kept at 30C for 2 h and then neutralized with MgO at from 20 to 25C, stirred for a further 6 h, filtered and then evaporated to about 450 g in a rotary evaporator at 80C and thereafter immediately poured into 1100 ml of methanol. The salt which crystallized out was filtered off, washed with methanol and dried.
220 g of individual corn-yellow crystals were obtained, corresponding to a yield of 87.7% of theory, based on ascorbic acid.
Analysis of the salt gave an atomic ratio of Xo~8Mgl~o6c56Hl2spl~ corresponding to the compound KMgC6H6PO9-3~2o .
.- ~ . . , 2~1292~
- 20 - O.Z. 0050/40665 According to HPLC analysis, the product contained 89.0% of ascorbate 2-phosphate and 9.9~ of bis-(2,2'-ascorbate) phosphate.
S To demonstrate the advantageous properties of the novel potassium magnesium L-ascorbate 2-phosphate com-pared with potassium L-ascorbate 2-phosphate and mag-nesium L-ascorbate 2-phosphate, the filtration resis-tance, the agglomeration on drying and the dust formation of potassium magnesium L-ascorbate 2-phosphates of the formula KrMgyC~H6POg~3H2O, ie. of potassium magnesium L-ascorbate 2-phosphates ha~ing different K/Mg ratio~, were compared with the corresponding properties of the potas-sium salts (x = 3, y = 0) or magnesium salts (x = 0, y =
1.5).
Experi- X Y Filtration Agglomeration Dust ment resistance on dryinq formation a) 0.00 1.50 +++ +++ +++
b) 0.08 1.46 +++ +++ +++
c) 0.17 1.~2 +++ ++ ++
d) 0.27 1.37 ++ ++ ++
e) 0.36 1.32 ++ + ++
f) 0.48 1.26 ~ + +
g) 0.61 1.20 - - +
h) 0.75 1.12 - - +
i) 0.83 1.09 - - +
j) 1.08 0.96 - - +
k) 1.20 0.86 - - +
l~ 1.54 0.73 + +
m) 1.86 Q.57 + +
n) 2.15 0.43 + ++
o) 3.00 0.00 Product obtained a~ an oil .
2~29~
- 21 - O.Z. 0050/~0665 The experiments showed that salts having the composition K1~03Mg1~0 lS ascorbate 2 phosphate have the best product properties.
Evaluation scale:
+++ Very great ++ Great + Average - Low
Claims (10)
1. A process for the preparation of ascorbic acid 2-phosphate by reacting ascorbic acid or an ascorbic acid derivative which has a group of the formula I
(I) where R1 and R2 are each hydrogen or together form one of the groups or with POCl3 in the presence of a tertiary amine in a suit-able aqueous solvent at 10 to 25°C while maintaining a pH of about 8-13.5, by adding KOH during he entire phosphorylation reaction, and then isolating the ascorbic acid 2-phosphate, wherein, to separate off the excess inorganic phosphate, about the stoichiometric amount of a magnesium compound, advantageously in the form of an aqueous solution, is added to the reaction mixture obtained in the phosphorylation, directly and without prior treatment with an ion exchanger, at a pH ~ 7, until the formation of crystalline KMgPO4 is complete, the KMgPO4 which is crystallized out is separated off and the ascorbic acid phosphate is isolated from the filtrate in a conventional manner.
(I) where R1 and R2 are each hydrogen or together form one of the groups or with POCl3 in the presence of a tertiary amine in a suit-able aqueous solvent at 10 to 25°C while maintaining a pH of about 8-13.5, by adding KOH during he entire phosphorylation reaction, and then isolating the ascorbic acid 2-phosphate, wherein, to separate off the excess inorganic phosphate, about the stoichiometric amount of a magnesium compound, advantageously in the form of an aqueous solution, is added to the reaction mixture obtained in the phosphorylation, directly and without prior treatment with an ion exchanger, at a pH ~ 7, until the formation of crystalline KMgPO4 is complete, the KMgPO4 which is crystallized out is separated off and the ascorbic acid phosphate is isolated from the filtrate in a conventional manner.
2. A process for the preparation of ascorbic acid 2-phosphate as claimed in claim 1, wherein A) the starting material used is an ascorbic acid derivative which has a group of the formula I where R1 and R2 are each hydrogen or together form one of the groups - 23 - O.Z. 0050/40665 or B) an aqueous solution of a magnesium compound is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgP04 is com-plete, C) the KMgP04 which is crystallized out is separated off, D) to separate off the inorganic potassium salts, the resulting filtrate is evaporated to a solids content of from 20 to 90% by weight at a pH of from 6 to 11 and cooled to a temperature of from -10 to +20°C
until the potassium salts have completely crystal-lized out, and E) the ascorbic acid phosphate is isolated in a conven-tional manner from the reaction solution which is obtained by separating off the inorganic potassium salts and substantially freed from inorganic salts.
until the potassium salts have completely crystal-lized out, and E) the ascorbic acid phosphate is isolated in a conven-tional manner from the reaction solution which is obtained by separating off the inorganic potassium salts and substantially freed from inorganic salts.
3. A process for the preparation of ascorbic acid 2-phosphate as claimed in claim 1, wherein A) the starting material used is an ascorbic acid derivative which has a group of the formula I where R1 and R2 together form one of the groups or B) an aqueous solution of a magnesium compound is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgPO4 is complete, C) the KMgPO4 which is crystallized out is separated off, 24 O.Z 0050/40665 D) to separate off the inorganic potassium salts, the resulting filtrate is evaporated down at from 0 to 60°C and at a pH of from 6 to 11, and from 0.1 to 5 times the amount, based on the evaporated filtrate, of a lower primary alkanol or acetone is added and the stirred mixture is cooled to a temperature of from -20 to +50°C until the potassium salts have completely crystallized out, and E) the ascorbic acid phosphate is isolated in a conven-tional manner from the reaction solution which is obtained by separating off the inorganic potassium salts and substantially freed from inorganic salts.
4. A process for the preparation of ascorbic acid 2-phosphate as claimed in claim 1, wherein the starting material used is an ascorbic acid derivative which has a group of the formula I where R1 and R2 together form the group and which was prepared by treatment, for from 1 to 8 hours at from -20 to +40°C, with a mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40°C while stirring, separating off the 5,6-isopropy-lideneascorbic acid which crystallizes out, at about -15°C, and pressing the crystals dry.
5. A process for the preparation of L-ascorbic acid 2-phosphate as claimed in claim 1, wherein A) L-ascorbic acid is treated, at from -10 to +10°C for from 5 to 6 hours, with a mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from-30 to +40°C, while stirring, and the 5,6-isopropy-lidene-L-ascorbic acid which crystallizes out is separated off at about -15°C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 - 25 - O.Z. 0050/40665 to 13.5 and in the presence of a tertiary amine at from -10 to +25°C in a suitable aqueous solvent, B) the aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgPO4 is complete, C) the KMgPO4 which is crystallized out is separated off, D) to separate off potassium chloride, the resulting filtrate is evaporated to a solids content of from 20 to 90% by weight at a pH of from 7 to 11 and cooled to a temperature of from -20 to +20°C until KCl has completely crystallized out, and E) the L-ascorbic acid phosphate is isolated in a conventional manner from the reaction solution obtained by separating off KCl and substantially freed from inorganic salts.
6. A process for the preparation of L ascorbic acid 2-phosphate as claimed in claim 1, wherein A) L-ascorbic acid is treated, at from -10 to +10°C for from 5 to 6 hours, with a mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40°C, while stirring, and the 5,6-isopropy-lidene-L-ascorbic acid which crystallizes out is separated off at about -15°C, pressed dry and then reacted with POC13 while maintaining a pH of from 8 to 13.5 by means of KOH and in the presence of a tertiary amine at from -10 to +25°C in a suitable aqueous solvent, B) the aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgPO4 is complete, C) the KMgPO4 which is crystallized out is separated off, - 26 - O.Z. 0050/40665 D) to separate off potassium chloride, the resulting filtrate is evaporated down at a pH of from 6 to 11, and from 0.1 to 5, preferably from 0.8 to 1.2, times the amount, based on the evaporated filtrate, of a lower alkanol or acetone is added and the mixture is cooled to 0-10°C until KCl has completely crystal-lized out, and E) the L-ascorbic acid phosphate is isolated in a conventional manner from the resulting reaction solution substantially freed from inorganic salts.
7. A process for the preparation of L-ascorbic acid 2-phosphate as claimed in claim 1, wherein A) L-ascorbic acid is treated, at from -10 to +10°C for from 5 to 6 hours, with a mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40°C while stirring, the 5,6-isopropylidene-L-ascorbic acid which crystallizes out is separated off at about -15°C, pressed dry and then reacted with POCl3 while maintaining a pH of from 8 to 13.5 by means of XOH and in the presence of a tertiary amine at from -10 to +25°C in a suitable aqueous solvent, B) an aqueous solution of magnesium chloride is added to the reaction mixture obtained in the phosphoryla-tion, without prior treatment with an ion exchanger, until the formation of crystalline KMgPO4 is complete, C) the KMgPO4 which is crystallized out is separated off, D) to separate off potassium chloride the resulting filtrate is evaporated down at a pH of from 6 to 11 and/or from 0.1 to 5, preferably from 0.8 to 1.2, times the amount, based on the filtrate a lower alkanol or acetone is added and the mixture is cooled to 0-10°C
until KCl has completely crystallized out, E) the resulting reaction solution which has been sub-stantially freed from inorganic salts is treated - 27 - O.Z. 0050/40665 with a moderately acidic cation exchanger which loses its exchange capacity at a pH of from about 2.0 to 0.5, and F) the L-ascorbic acid 2-phosphate is precipitated in the form of the novel potassium magnesium ascorbate 2-phosphate from the resulting reaction mixture essentially containing the monopotassium salt of L-ascorbic acid 2-phosphate, by adding MgO, Mg(OH)2 or MgCO3 until the solution has a pH of about 7 and if necessary treating the solution with methanol or acetone.
until KCl has completely crystallized out, E) the resulting reaction solution which has been sub-stantially freed from inorganic salts is treated - 27 - O.Z. 0050/40665 with a moderately acidic cation exchanger which loses its exchange capacity at a pH of from about 2.0 to 0.5, and F) the L-ascorbic acid 2-phosphate is precipitated in the form of the novel potassium magnesium ascorbate 2-phosphate from the resulting reaction mixture essentially containing the monopotassium salt of L-ascorbic acid 2-phosphate, by adding MgO, Mg(OH)2 or MgCO3 until the solution has a pH of about 7 and if necessary treating the solution with methanol or acetone.
8. Potassium magnesium L-ascorbate 2-phosphate.
9. K1?03Mg1?0.15 L-ascorbate 2-phosphate.
10. A process for the preparation of 5,6-isopropy-lideneascorbic acid by reacting ascorbic acid with ace-tone, wherein the ascorbic acid is treated, at from -10 to +10°C for from S to 6 hours, with a mixture obtained by adding from 0 to 65% strength by weight oleum to acetone containing from 0 to 5% by weight of water at from -30 to +40°C while stirring, and the 5,6-isopropy-lideneascorbic acid which crystallizes out is separated off at about -15°C, if necessary after washing with ice-cooled acetone.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002012926A CA2012926A1 (en) | 1989-03-21 | 1990-03-23 | Preparation of ascorbic acid 2-phosphate and of 5,6- isopropylideneascorbic acid and potassium magnesium l-ascorbate 2-phosphate as an advantageous salt of l-ascorbic acid 2-phosphate |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3909198A DE3909198A1 (en) | 1989-03-21 | 1989-03-21 | METHOD FOR THE PRODUCTION OF ASCORBIN ACID-2-PHOSPHATE AND 5,6-ISORPROPYLIDENE-ASCORBIN ACID AS A BASE PRODUCT |
| CA002012926A CA2012926A1 (en) | 1989-03-21 | 1990-03-23 | Preparation of ascorbic acid 2-phosphate and of 5,6- isopropylideneascorbic acid and potassium magnesium l-ascorbate 2-phosphate as an advantageous salt of l-ascorbic acid 2-phosphate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2012926A1 true CA2012926A1 (en) | 1991-09-23 |
Family
ID=25674026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002012926A Abandoned CA2012926A1 (en) | 1989-03-21 | 1990-03-23 | Preparation of ascorbic acid 2-phosphate and of 5,6- isopropylideneascorbic acid and potassium magnesium l-ascorbate 2-phosphate as an advantageous salt of l-ascorbic acid 2-phosphate |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2012926A1 (en) |
-
1990
- 1990-03-23 CA CA002012926A patent/CA2012926A1/en not_active Abandoned
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