US3923874A - Continuous production of esters of glycols or their monoethers with lower fatty acids - Google Patents

Continuous production of esters of glycols or their monoethers with lower fatty acids Download PDF

Info

Publication number
US3923874A
US3923874A US367327A US36732773A US3923874A US 3923874 A US3923874 A US 3923874A US 367327 A US367327 A US 367327A US 36732773 A US36732773 A US 36732773A US 3923874 A US3923874 A US 3923874A
Authority
US
United States
Prior art keywords
glycol
entrainer
ester
water
zone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US367327A
Other languages
English (en)
Inventor
Heinz Hohenschutz
Paul Hornberger
Josef Gnad
Guenter Dinkhauser
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE19722228335 external-priority patent/DE2228335C3/de
Application filed by BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of US3923874A publication Critical patent/US3923874A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
    • G—PHYSICS
    • G08—SIGNALLING
    • G08B—SIGNALLING OR CALLING SYSTEMS; ORDER TELEGRAPHS; ALARM SYSTEMS
    • G08B17/00—Fire alarms; Alarms responsive to explosion
    • G08B17/06—Electric actuation of the alarm, e.g. using a thermally-operated switch

Definitions

  • HOA-X (l) in which A is ethylene, propylene or butylene; and X is OH or OR in which R is alkyl of one to four carbon atoms or OAOH or OAOR in which A and R have the meanings given above with a lower saturated fatty acid at elevated temperature in the presence of a catalytic amount of a strong acid while continuously removing the water formed by means of an entrainer followed by treatment with an aqueous alkali.
  • the glycol of the formula (1) is reacted in a first zone with the lower fatty acid, the water formed being distilled off as an azeotrope over the top by means of an entrainer.
  • glycol ester including the entrainer is removed from the bottoms, mixes with an aqueous alkali, extracted in a second zone while supplying an extractant and water with phase "separation and in a third zone the pure glycol ester is recovered from the resulting mixture of glycol ester.
  • entrainer and extractant by rectification.
  • Glycol esters are used as solvents for surface coating agents.
  • carboxylic esters are obtained by heating mixtures of carboxylic acids and alcohols in the presence of strong acids as catalysts and continuously removing the water formed (compare Houben-Weyl, Methoden der organischen Chemie, volume 8, 1952, pages 516 et seq.).
  • the crude carboxylic esters are worked up as a rule by neutralization with aqueous alkalies followed by distillation. This procedure cannot be carried out in the production of wholly or partly water-soluble esters, for example in the case of esters of lower glycols or glycol alkyl ethers because in the treatment with aqueous alkalies considerable quantities of useful products pass into the waste water.
  • Solid neutralization agents which are insoluble in the ester are therefore usually employed and this has the disadvantage that encrustation of the evaporator takes place in the subsequent distillation.
  • washing with aqueous alkalies is dispensed with and the useful products are distilled from the reaction mixture containing acid. This method has the disadvantage that apparatus used for the purifying distillation of the glycol esters is corroded.
  • HO-A-X in which A is ethylene, propylene or butylene and X is OH or OR in which R is alkyl of one to four carbon atoms, or OAOH orOAOR in which A and R have the above meanings, witha lower saturated fatty acid at elevated temperature in the presence of a catalytic amount of a strong acid with continuous removal of water by entrainment followed by treatment with an aqueous alkali, wherein the improvement consists in reacting the glycol of the formula (I) with the lower fatty acid in a first zone in which the water formed is distilled azeotropically by means of an entrainer over the top and the crude glycol ester including entrainer is withdrawn from the bottoms, adding aqueous alkali, extracting the ester in a second zone with the supply of extractant and water with phase separation, and recovering the pure glycol ester by rectification of the resulting mixture of glycol ester, entrainer and extractant in a third zone.
  • HO-AX in which A is ethylene, propylene or butylene and X is OH, OR where R is alkyl of one to four carbon atoms, OAOH or OAOR where A and R have the above meanings with a lower fatty acid at elevated temperature in the presence of a catalytic amount of a strong acid with continuous removal of the water formed by means of an entrainer followed by treatment with an aqueous alkali, when in a first zone the glycol of the formula (I) is reacted with the lower fatty acid in the presence of a catalytic amount of a strong acid, the water formed being simultaneously distilled off over the top by means of an entrainer and the crude glycol ester including the entrainer being withdrawn from the bottoms, the ester is mixed with an aqueous alkali and extracted in a second zone while supplying extractant and water with phase separation, and in a third zone the pure glycol ester is recovered by rectification from the mixture of glycol ester, entrain
  • the new process has the advantage that encrustation and corrosion phenomena do not occur in the distillation of the pure ester. Moreover the new process has the advantage that useful products are not discharged with the effluent.
  • glycols of the formula (I) are ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether and diethylene glycol monomethyl ether.
  • Lower fatty acids of one to four carbon atoms such as formic acid, acetic acid, propionic acid and butyric acid are preferred.
  • glycol of formula (I) and the lower saturated fatty acid are generally used in stoichiometric ratio.
  • An excess of glycol of up to preferably 5 percent by weight may be used.
  • the reaction is carried out in a first zone in the presence of a catalytic amount of a strong acid, the water formed being taken overhead by means of an entrainer.
  • Suitable entrainers are those which form an azeotrope with water out not with the glycol esters.
  • the boiling point of the entrainer used should be as far as possible below that of the ester to be prepared.
  • suitable entrainers are hydrocarbons such as benzene or toluene.
  • Esters of alkanols of one to five carbon atoms with fatty acids of one to four carbon atoms, particularly acetic acid, such as ethyl, propyl, butyl and pentyl acetate, are preferred.
  • the entrainer is conveniently used in an amount of from 20 to percent by weight based on the crude ester.
  • the reaction is carried out in the presence of a strong acid present in a catalytic amount.
  • a strong acid present in a catalytic amount.
  • non-oxidizing strong mineral acids such as hydrochloric acid, sulfuric acid, phosphoric acid or organic sulfonic acids such as benzenesulfonic acid or toluenesulfonic acid.
  • the said acids are advantageouslyused in amounts of from 0.1 to 2 percent and particularly from 0.5 to 1.5 percent by weight based on the mixture of glycols and lower fatty acids.
  • the first zone may conveniently be a rectifying zone.
  • Conventional rectifying columns may advantageously be used for the purpose. Packed columns or plate columns have proved to be particularly suitable. The columns used advantageously have from to 35 theoretical plates.
  • the temperature in the bottoms is kept as a rule at from 130 to 160C, while the top temperature is adjusted according to the boiling point of the entrainer used.
  • the mixture of crude glycol ester and entrainer obtained is mixed with an aqueous alkali.
  • suitable alkalies are caustic soda solution, cau'stic potash solution and sodium carbonate solution.
  • the alkali is conveniently used as a 4 to 8 percent by weight solution. It is advantageous to use from 1.2 to 2.0 and particularly from 1.4 to 1.6 times the stoichiometric amount of alkali based on the acid used as catalyst.
  • the crude glycol ester and the aqueous alkali are advantageously mixed in a tubular zone in which intense mixing takes place.
  • the treatment is carried out as a rule at a temperature of from 20 to 60C.
  • the mixture of aqueous alkali, crude glycol ester and entrainer thus obtained is extracted in a second zone with the supply of an extractant and water with phase separation.
  • the second zone may conveniently be an extractive column, for example a pulse column.
  • the said mixture is advantageously supplied in the middle and water at the top of the column while extractant is introduced in the lower third.
  • the wash water is removed at the lower end.
  • the upper organic phase which contains crude glycol ester devoid of acid, is taken overhead.
  • Suitable extractants include hydrocarbons such as benzene or toluene and also esters of alkanols of one to five carbon atoms with fatty acids of one to four carbon atoms and particularly acetates such as ethyl acetate or butyl acetate. It is advantageous for the extractant to have a substantially lower boiling point than the glycol ester to be prepared. It has proved to be particularly convenient for the extractant to be identical with the entrainer. It is advantageous to supply such an amount of the extractant that the organic phase removed contains from 30 to 170 percent and particularly from 50 to 100 percent of extractant inclusive of entrainer and based on the crude esterjThe extraction is generally carried out at from 20 to 40C.
  • the amount of wash water used is generally from 5 to 20 percent by weight based on the crude ester.
  • the pure glycol ester is recovered by rectification in a third zone from the resulting mixture of ester and extractant including entrainer and it is convenient to distil off the extractant and entrainer together with residual water over the top while the pure glycol ester is preferably removed in the lower third of the column.
  • Conventional columns for example packed columns or plate columns preferably having from to 40 theoretical plates may conveniently be used for the final distillation.
  • the process of the invention may for example be carried out, as shown in FIG. 1, by supplying glycol at lower fatty acid at 2 and strong mineral acid at 3 through a line 4 to a column K1, while some of the extractant/entrainer is introduced through line 5 into column K1.
  • An azeotrope of water and entrainer is withdrawn at the top of the column through line 16 and is separated in a separator 17 into two phases, the entrainer being returned through line 18 into column Kl while the water passes through line 7 to a mixing chamber 19. Crude glycol ester mixed with the entrainer and extractant is withdrawn from column Kl through line 6.
  • Aqueous alkali in container 19 is diluted through line 8 with water and supplied through line 9 to the crude glycol ester and the mixture is supplied to extractive column K2 through line 6 already mentioned.
  • Water is supplied through line 10 to the top of extractive column K2, extractant is supplied through line 15 to the lower third, while water is withdrawn at the lower end through line 24.
  • the organic phase forming in the upper portion of extractive column K2 is passed through line 20 into a distillation column K3 where a mixture of extractant/entrainer is withdrawn as an azeotrope with water at the top through line 21; the water is separated in the separator 22 and returned through line 14 into the mixing vessel 19 while the extractantlentrainer is returned through line 23 into column K3 as a reflux, but the major portion is supplied through line 5 again to column K1 and line 15 to extraction column K2. Pure glycol ester is withdrawn through line 12 in the lower third and high boiling point byproducts are withdrawn from the bottoms through line 13.
  • glycol esters thus prepared have low acid numbers of from 0.01 to a maximum of 0.1.
  • the content of glycol ester prepared in this way is always more than 99.5 percent by weight.
  • the glycol esters prepared according to the invention are excellent solvents and are suitable inter alia in the processing of polyurethane and nitrocellulose coating agents.
  • EXAMPLE 1 A mixture of 680 parts per hour of acetic acid and 870 parts per hour of ethylene glycol monomethyl ether is metered together with 28.5 parts per hour of sulfuric acid and 1,300 parts per hour of isobutyl acetate (obtained from the pure ester column) into an esterification column. The water is entrained out over the top. The temperature at the top of the column is 93C and in the bottoms it is from to C. The crude ester is neutralized with 620 parts of an 8% sodium carbonate solution and washed in a washing column to which 250 parts per hour of water is fed at the top.
  • the lower part of the wash column serves as the extractive portion into which 700 parts per hour of isobutyl acetate (also withdrawn as a reflux from the pure ester column) is introduced.
  • the neutralized and washed crude ester which contains 60 percent of isobutyl acetate flows into the pure ester column from which 1,295
  • EXAMPLE 2 As described in Example 1 a mixture of 415 parts per hour of acetic acid, 840 parts per hour of butyl glycol (ethylene glycol monobutyl ether) and 25.4 parts per hour of sulfuric acid is metered together with 1,000 parts per hour of isobutyl acetate into the esterification column. A temperature of 93C is set up at the top of the column and of 155 to 160C in the bottoms. Neutralization is carried out with 585 parts of 5 percent caustic soda solution. 200 parts per hour of isobutyl acetate is used for extraction and 200 parts of water per hour is passed into the extractive column.
  • the organic phase from the extractive column is passed into the pure ester column and fractionally distilled.
  • the butyl glycol acetate is withdrawn as a vapor from the lower part of the pure ester column at 200 mm Hg and 144C at the rate of 1,110 parts per hour corresponding to a yield of 98.3 percent based on the acetic acid used.
  • the yield based on butyl glycol is 97.4 percent of theory.
  • EXAMPLE 3 A mixture of 555 parts per hour or propionic acid and 690 parts of ethyl glycol (ethylene glycol monoethyl ether) is esterified as described in Example 1 in the presence of 24.7 parts of sulfuric acid at 150 to 160C. Toluene serves as extractant. 975 parts per hour is returned to the esterification column and 450 parts per hour of toluene into the extractive portion. 1,060 parts per hour of ethyl glycol propionate is withdrawn at 140C and 220 mm Hg from the pure ester column; this is equivalent to a yield of 97.2 percent based on propionic acid. The yield based on ethyl glycol is 96.8 percent of theory.
  • ethyl glycol ethylene glycol monoethyl ether
  • EXAMPLE 4 450 parts per hour of acetic acid and 910 parts per hour of methyldiethylene glycol (diethylene glycol monomethyl ether) are esterified as described in Example 1 in the presence of 26 parts per hour of sulfuric acid at 160 to 165C.
  • the amount of butyl acetate for the esterification column is 1,300 parts per hour and for the extractive column 640 parts per hour.
  • At 160C and 200 mm Hg 1,185 parts per hour of methyldiethyleneglycol acetate is withdrawn from the pure ester column, equivalent to a yield of 96.8 percent based on acetic acid.
  • the yield based on methyldiethylene glycol is 96.5 percent of theory.
  • a process for the continuous production of wholly or substantially water-soluble esters of glycols or of their monoethers with lower fatty acids which process comprises:
  • A is ethylene, propylene or butylene
  • X is OH, OR, OAOH or OAOR wherein R is alkyl of one to four carbon atoms and A has the above meaning, with a lower saturated fatty acid at an elevated temperature and in the presence of a catalytic amount of a strong acid while the water formed in the reaction is simultaneously distilled off azeotropically over the top by means of an entrainer which forms an azeotrope with water selected from the group consisting of hydrocarbons and lower fatty acid esters of alkanols of l to 5 carbon atoms, said entrainer being continuously introduced into said first zone and the crude glycol ester mixed with entrainer being continuously withdrawn from the bottom of said first zone;
  • glycol used is ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether or diethylene glycol monomethyl ether.
  • a process as claimed in claim 1 wherein the fatty acid reacted with the glycol has one to four carbon atoms.
  • a process as claimed in claim 1 wherein the treatment with an alkali is carried out at a temperature of from 20 to 60C.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Business, Economics & Management (AREA)
  • Emergency Management (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
US367327A 1972-06-10 1973-06-06 Continuous production of esters of glycols or their monoethers with lower fatty acids Expired - Lifetime US3923874A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19722228335 DE2228335C3 (de) 1972-06-10 Verfahren zur kontnuierlichen Herstellung von Estern von Glykolen oder deren Monoäthern mit niedermolekularen Fettsäuren

Publications (1)

Publication Number Publication Date
US3923874A true US3923874A (en) 1975-12-02

Family

ID=5847384

Family Applications (1)

Application Number Title Priority Date Filing Date
US367327A Expired - Lifetime US3923874A (en) 1972-06-10 1973-06-06 Continuous production of esters of glycols or their monoethers with lower fatty acids

Country Status (7)

Country Link
US (1) US3923874A (nl)
JP (1) JPS4961115A (nl)
BE (1) BE800696A (nl)
FR (1) FR2187757B1 (nl)
GB (1) GB1422879A (nl)
IT (1) IT988741B (nl)
NL (1) NL185075C (nl)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4544453A (en) * 1983-03-17 1985-10-01 Atlantic Richfield Company Stripping of unreacted glycol ethers and acids from an esterification reaction mixture

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3475188D1 (nl) * 1983-03-17 1988-12-22 Atlantic Richfield Company
US5618973A (en) * 1994-11-10 1997-04-08 Union Carbide Chemicals & Plastics Technology Corporation Esterification process
GB2312673A (en) * 1995-05-01 1997-11-05 Occidental Chem Co Glycol ether acetate preparation

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1972579A (en) * 1933-05-12 1934-09-04 Carbide & Carbon Chem Corp Esters of 2-ethylbutanol-1
US2757157A (en) * 1950-09-07 1956-07-31 Sun Oil Co Esters of pentanediols and their use as plasticizers for vinyl-type polymers
US2871248A (en) * 1955-10-31 1959-01-27 American Oil Co Glycol diesters
US2920056A (en) * 1957-06-06 1960-01-05 Exxon Research Engineering Co Plasticizer from polymethylol alkanes and 3-alkyl alkanoic acids and polymeric compositions containing same
US3023185A (en) * 1956-09-04 1962-02-27 Exxon Research Engineering Co Plasticizers for vinyl-type resins
US3053883A (en) * 1960-06-22 1962-09-11 Ici Ltd Use of metal salts to promote esterification

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE975700C (de) * 1962-05-10 Chemische Werke Hüls Aktiengesellschaft Marl (Kr Recklmghausen) Verfahren zur Herstellung von reinen Carbonsaureestern
DE860353C (de) * 1939-07-21 1952-12-22 Hoechst Ag Verfahren zur ununterbrochenen Herstellung von Carbonsaeureestern

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1972579A (en) * 1933-05-12 1934-09-04 Carbide & Carbon Chem Corp Esters of 2-ethylbutanol-1
US2757157A (en) * 1950-09-07 1956-07-31 Sun Oil Co Esters of pentanediols and their use as plasticizers for vinyl-type polymers
US2871248A (en) * 1955-10-31 1959-01-27 American Oil Co Glycol diesters
US3023185A (en) * 1956-09-04 1962-02-27 Exxon Research Engineering Co Plasticizers for vinyl-type resins
US2920056A (en) * 1957-06-06 1960-01-05 Exxon Research Engineering Co Plasticizer from polymethylol alkanes and 3-alkyl alkanoic acids and polymeric compositions containing same
US3053883A (en) * 1960-06-22 1962-09-11 Ici Ltd Use of metal salts to promote esterification

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4544453A (en) * 1983-03-17 1985-10-01 Atlantic Richfield Company Stripping of unreacted glycol ethers and acids from an esterification reaction mixture

Also Published As

Publication number Publication date
IT988741B (it) 1975-04-30
DE2228335A1 (de) 1974-04-18
FR2187757B1 (nl) 1977-02-11
FR2187757A1 (nl) 1974-01-18
NL185075B (nl) 1989-08-16
NL7307701A (nl) 1973-12-12
JPS4961115A (nl) 1974-06-13
DE2228335B2 (de) 1976-12-23
NL185075C (nl) 1990-01-16
BE800696A (fr) 1973-12-10
GB1422879A (en) 1976-01-28

Similar Documents

Publication Publication Date Title
US4544776A (en) Process for separating methanol from the reaction products obtained in the etherification of C4 through C7 isoolefins with methanol
JP3346822B2 (ja) アクリル酸エステル又はメタクリル酸エステルの製造法
EP0449913A1 (de) Verfahren zur verbesserten herstellung von (meth)acrylsäureestern mehrwertiger alkohole (iii).
JPH09110789A (ja) （メタ）アクリル酸のアルキルエステルを連続的に製造するための方法及び装置
KR100762773B1 (ko) 연속식 에틸 락테이트 제조 방법
US4329492A (en) Process for production of methacrylic acid esters
EP0023119B1 (en) Process for preparation of high purity isobutylene
CN104761452B (zh) 一种丙烯酸丁酯粗产品的纯化方法
US3923874A (en) Continuous production of esters of glycols or their monoethers with lower fatty acids
KR0184885B1 (ko) 4-하이드록시부틸 (메트)아크릴레이트의 제조방법
JP2004529203A (ja) （メタ）アクリル酸エステルの製造方法
JP2002511081A (ja) 不飽和ジカルボン酸無水物のジメチルエステルを生成する方法
DE2635566C3 (de) Verfahren zur Herstellung von Oxiranverbindungen durch Cracken eines entsprechenden Alkylenglykolmonoesters
US3576890A (en) Process for the preparation of alkylene glycols
US6472554B1 (en) Continuous preparation of alkyl esters of (meth) acrylic acid
US3640851A (en) Purification of dehydrolinalool by fractional distillation and water washing
US2649475A (en) Process for the manufacture of methyl acrylate
US3959389A (en) Method of manufacturing alkylene oxide adducts of an aliphatic alcohol
GB2207914A (en) Process for the production of a mixture of butane 1,4-diol gamma-butyrolactone and tetrahydrofuran
US3637751A (en) Production of trioxane
JPH09328451A (ja) Ｈｆ触媒を用いたカルボン酸エステルの製造方法
JP2001508414A (ja) （メタ）アクリル酸エステルの製法
JPH05186391A (ja) 酢酸エチルの精製法
US3555078A (en) Process of manufacturing aliphatic esters
US3932531A (en) Method of manufacturing alkylene oxide adducts of an aliphatic alcohol