CN112877372B - Process for preparing tertiary alpha-aryl cyclic ketones - Google Patents
Process for preparing tertiary alpha-aryl cyclic ketones Download PDFInfo
- Publication number
- CN112877372B CN112877372B CN202110190279.4A CN202110190279A CN112877372B CN 112877372 B CN112877372 B CN 112877372B CN 202110190279 A CN202110190279 A CN 202110190279A CN 112877372 B CN112877372 B CN 112877372B
- Authority
- CN
- China
- Prior art keywords
- reaction
- cyclic ketone
- aryl cyclic
- tertiary alpha
- preparation
- 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.)
- Active
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
- C12P7/26—Ketones
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Materials Engineering (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention provides a preparation method of tertiary alpha-aryl cyclic ketone, which comprises an intermediate product preparation step and a tertiary alpha-aryl cyclic ketone preparation step, wherein the intermediate product preparation step comprises the steps of sequentially adding 2-iodo-2-cyclohexenone, a phenylboronic acid derivative, alkali, a Pd catalyst and a solvent, stirring for coupling reaction to obtain a reaction solution with a generated intermediate product, the tertiary alpha-aryl cyclic ketone preparation step comprises a first mode or a second mode, wherein the first mode comprises the steps of regulating the pH of the reaction solution, adding freeze-dried powder containing whole cells of old yellow enzyme and glucose dehydrogenase, adding NADPH and glucose for reaction after the cells are suspended and dispersed again, extracting and drying after the reaction is finished, and performing silica gel column chromatography to obtain the tertiary alpha-aryl cyclic ketone after the filtration and the desolventization. The preparation method of the tertiary alpha-aryl cyclic ketone can utilize the chemical-enzymatic method to asymmetrically catalyze to obtain the optically active tertiary alpha-aryl cyclic ketone containing the chiral center, and has good application effect.
Description
Technical Field
The invention relates to the technical field of compound preparation, in particular to a preparation method of tertiary alpha-aryl cyclic ketone.
Background
The tertiary alpha-aryl cyclic ketone is an important structural unit in medicines, bioactive molecules and natural products, and is a synthetic object with great attractiveness due to wide application. However, the synthetic approaches to tertiary alpha-aryl cyclic ketones are very limited compared to their widespread use.
Asymmetric alpha-arylation of carbon-based compounds is one of the most effective means for synthesizing optically active alpha-aryl cyclic ketones, but this means is often used for synthesizing quaternary alpha-aryl cyclic ketones. For the synthesis of the tertiary alpha-aryl compound, on one hand, the tertiary alpha-aryl compound contains acidic alpha-H and can undergo racemization reaction under alkaline environment, so that the means is limited, and in the prior literature report, the bridge ring framework is constructed while the tertiary alpha-aryl cyclic ketone is synthesized mainly through dynamic kinetic resolution and desymmetry reaction so as to effectively avoid racemization by utilizing the rigid bicyclic structure of the tertiary alpha-aryl cyclic ketone. On the other hand, when an optically active α -aryl cyclic ketone is synthesized by asymmetric α -arylation reaction of a carbon-based compound, polyarylation and aldol condensation reaction also occur when a ketone substrate having a small number of arylation substituents is arylated. In the prior art, the slightly alkaline enol compound is mainly used to effectively prevent the polyarylation and aldol condensation reaction.
In addition to the above asymmetric alpha-arylation reactions of carbon-based compounds, lewis acid is currently used for assistanceThe asymmetric protonation reaction of the acid catalyst on the achiral enol compound can also realize the high-efficiency synthesis of the alpha-phenyl cyclic ketone. Meanwhile, the asymmetric epoxidation of benzyl cyclobutane and the rearrangement reaction of epoxy compound also realize the more challenging asymmetric synthesis of tertiary alpha-aryl cyclopentanone.
However, the direct catalytic synthesis of optically active α -aryl cyclic ketones using ketone compounds as substrates still faces a great limitation. Although asymmetric hydrogenation of simple, readily available achiral enol compounds using transition metals or organic catalysts is considered the most straightforward and simple method for the synthesis of chiral ketones, great progress has been made in the study of hydrogenation of acyclic and exocyclic enones.
However, few studies have been made on cyclic enones, particularly on α -substituted substrates, as yet unreported, and asymmetric hydrogenation of α -aryl cyclic enones remains a challenging goal, both in chemical and biocatalysis. In addition, while chemo-enzymatic catalysis coupled with broad catalytic capabilities of chemical catalysts and precise selectivity of biocatalysts provides a new approach to asymmetric synthesis, the instability of biocatalysts and incompatibility between the two catalytic domains make this concept still very challenging.
Disclosure of Invention
In view of the above, the present invention is directed to a method for preparing a tertiary α -aryl cyclic ketone, so as to prepare the tertiary α -aryl cyclic ketone.
In order to achieve the purpose, the technical scheme of the invention is realized as follows:
a process for preparing a tertiary α -aryl cyclic ketone, the process comprising:
a. an intermediate preparation step, and the intermediate preparation step comprises:
sequentially adding 2-iodine-2-cyclohexenone, a phenylboronic acid derivative, alkali, a Pd catalyst and a solvent into a reaction vessel, and stirring at 60-80 ℃ for coupling reaction for 4-12h to obtain a reaction solution with a generated intermediate product;
b. a tertiary alpha-aryl cyclic ketone preparation step, and the tertiary alpha-aryl cyclic ketone preparation step includes the following mode one or mode two, wherein:
the first mode comprises the following steps:
b11. b, when the reaction liquid in the step a is reduced to room temperature, adjusting the pH value of the reaction liquid to 6-8;
b12. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to make the cells re-suspended and dispersed;
b13. adding NADPH and glucose into the reaction solution, and stirring at 25-35 ℃ for reaction for 6-18h;
b14. after the reaction is finished, extracting and drying, and after the extraction filtration and the desolventization, carrying out silica gel column chromatography to obtain the tertiary alpha-aryl cyclic ketone in a white solid state;
the second mode includes:
b21. b, extracting the reaction liquid in the step a by using dichloromethane, drying by using anhydrous magnesium sulfate, and separating and purifying to obtain a generated intermediate product;
b22. dissolving the separated and purified intermediate product in a solvent to obtain a reaction solution;
b23. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to make the cells re-suspended and dispersed;
b24. adding NADPH and glucose into the reaction solution, and stirring at 25-30 ℃ to react for 6-18h;
b25. after the reaction is finished, extracting and drying are carried out, and after the extraction filtration and the desolventization, the tertiary alpha-aryl cyclic ketone in white solid is obtained by silica gel column chromatography.
Further, the phenylboronic acid derivative is one of phenylboronic acid, 2-methylphenylboronic acid, 3-methylphenylboronic acid, 4-chlorophenylboronic acid, 2-methyl-4-chlorophenylboronic acid, 4-methoxyphenylboronic acid and 2-naphthylboronic acid.
Further, the alkali is alkali metal hydroxide or alkali metal carbonate.
Further, the preparation of the Pd catalyst comprises:
c1. preparing an aminated modified magnetic mesoporous silica nanoparticle;
c2. dissolving magnetic mesoporous silica nanoparticles in deionized water, and performing ultrasonic dispersion to obtain a mixed solution;
c3. pd precursor NaPdCl 4 Dissolving in deionized water, dripping into the mixed solution, and stirring at 30 deg.C for reaction;
c4. reacting NaBH 4 Dissolving in deionized water, dripping into the mixed solution, and continuously stirring at 30 ℃ for reaction;
c5. after the reaction is finished, pd @ MMSN is obtained through magnetic separation.
Further, the solvent is DMF, DMSO, DME, THF, acetone, n-hexane, isooctane, ionic liquid [ BMIm][PF 6 ]And ionic liquids [ BMIm][NTF 2 ]A mixed solvent composed of one of the above and a buffer solution.
Further, in the step a, the concentration of the added 2-iodo-2-cyclohexenone is 5-50mM, the molar ratio of the added 2-iodo-2-cyclohexenone to the Pd catalyst is 1.
Further, in the step a, the concentration of the added 2-iodo-2-cyclohexenone is 25mM, the molar ratio of the added 2-iodo-2-cyclohexenone to the Pd catalyst is 1;
in step b, the pH of the reaction solution was adjusted to 7 in step b11, and the reaction was stirred at 30 ℃ for 12 hours after the addition of NADPH and glucose in steps b13 and b24.
Furthermore, after freeze-dried powder containing whole cells of the old yellow enzyme and the glucose dehydrogenase is added, the cells are repeatedly blown by a pipette gun to be resuspended and dispersed.
Further, the ratio of petroleum ether to ethyl acetate in the silica gel column is 10.
In step b, step b14 and step b25 are carried out by extracting with dichloromethane after the reaction is finished, and drying with anhydrous magnesium sulfate.
Compared with the prior art, the invention has the following advantages:
the preparation method of the tertiary alpha-aryl cyclic ketone takes 2-iodine-2-cyclohexenone which is simply and easily prepared as a substrate, generates an intermediate product through a Suzuki-Miyaura coupling reaction catalyzed by palladium, introduces aryl to an alpha position through a Suzuki-Miyaura cross coupling reaction catalyzed by Pd in the reaction process through an enzyme-catalyzed asymmetric hydrogenation reaction, and constructs a stereo center containing acidic alpha-H through asymmetric hydrogenation of ketene catalyzed by old yellow enzyme, so that the optically active tertiary alpha-aryl cyclic ketone containing a chiral center can be obtained through the chemical-enzyme method asymmetric catalysis.
The preparation method disclosed by the invention has the advantages that the carbonyl group does not need to be protected in the reaction process, the optical purity of the product is high, and the preparation method is a novel preparation method which is efficient, high in selectivity, good in operability and environment-friendly in yield. And particularly, when the mode I is adopted in the step b, the optically active tertiary alpha-aryl cyclic ketone containing the chiral center can be efficiently and selectively prepared in one pot, the yield is higher than that of a two-step two-pot mode, the complicated separation step of an intermediate product can be avoided, and the application effect is good.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate an embodiment of the invention and, together with the description, serve to explain the invention and not to limit the invention. In the drawings:
FIG. 1 is a reaction sequence for the preparation of tertiary alpha-aryl cyclic ketones according to an embodiment of the present invention;
FIG. 2 is an SEM image of a Pd catalyst prepared by the embodiment of the invention;
FIG. 3 is a TEM-Mapping image of Pd catalyst prepared by the inventive example.
Detailed Description
It should be noted that the embodiments and features of the embodiments may be combined with each other without conflict.
In addition, unless otherwise specified, all terms and processes related to the present embodiment should be understood according to the conventional knowledge and conventional methods in the art.
The present invention will be described in detail below with reference to the embodiments with reference to the attached drawings.
This example relates to a process for the preparation of a tertiary alpha-aryl cyclic ketone, which, in overall design, includes an intermediate preparation step a and a tertiary alpha-aryl cyclic ketone preparation step b.
Wherein, for the intermediate product preparation step a, the step specifically comprises:
adding 2-iodine-2-cyclohexenone, a phenylboronic acid derivative, alkali, a Pd catalyst and a solvent into a reaction vessel in sequence, and stirring at 60-80 ℃ for coupling reaction for 4-12h to obtain a reaction solution with a generated intermediate product.
In the above step, the phenylboronic acid derivative may be one of phenylboronic acid, 2-methylphenylboronic acid, 3-methylphenylboronic acid, 4-chlorophenylboronic acid, 2-methyl-4-chlorophenylboronic acid, 4-methoxyphenylboronic acid and 2-naphthylboronic acid.
As the alkali, an alkali metal hydroxide or an alkali metal carbonate can be used, and as the above alkali metal hydroxide, for example, potassium hydroxide or sodium hydroxide can be used, and as the above alkali metal carbonate, for example, potassium carbonate or sodium carbonate can be used.
The Pd catalyst is prepared by using NaPdCl as Pd precursor 4 By NaBH 4 And (3) in-situ reduction of the Pd catalyst product on the mesoporous channel of the aminated silicon-based material. Moreover, the silicon-based material in the amination modified silicon-based material can be inorganic silicon, organic silicon or organic-inorganic hybrid silicon in general, and preferably, siliconThe base material adopts Magnetic Mesoporous Silica Nanoparticles (MMSN).
Taking an example of an optimal magnetic mesoporous silica nanoparticle, the preparation of the Pd catalyst of this embodiment specifically includes the following steps:
c1. preparing an aminated modified magnetic mesoporous silica nanoparticle;
c2. dissolving magnetic mesoporous silica nanoparticles in deionized water, and performing ultrasonic dispersion to obtain a mixed solution;
c3. pd precursor NaPdCl 4 Dissolving in deionized water, dropwise adding into the mixed solution, and stirring at 30 deg.C for reaction;
c4. reacting NaBH 4 Dissolving in deionized water, dripping into the mixed solution, and continuously stirring at 30 ℃ for reaction;
c5. after the reaction is finished, pd @ MMSN is obtained through magnetic separation.
In the above Pd catalyst preparation process, the magnetic mesoporous silica nanoparticles can be synthesized, for example, according to literature (j.gao, w.kong, l.zhou, y.he, l.ma, y.yun, l.yan, y.jiang, chem.eng.j.2017,309, 70). And the amination modification of the prepared magnetic mesoporous silica nanoparticles specifically comprises the steps of adding the magnetic mesoporous silica nanoparticles and n-hexane into a reactor, adding 3-Aminopropyltriethoxysilane (APTES) after ultrasonic treatment, then placing the reactor into a water bath kettle at 80 ℃, and condensing and refluxing for 12 hours to obtain a product. Then separating the product by using a magnet, and washing the product by using absolute ethyl alcohol and ultrapure water for three times respectively to obtain the aminated MMSN.
Furthermore, it should be noted that in the preparation of the Pd catalyst, the NaPdCl precursor is added by adjusting the amount of Pd precursor added 4 While different Pd-supported Pd catalysts can be obtained, it is preferred to use 10% supported Pd catalyst in this example.
In this embodiment, the solvent is DMF, DMSO, DME, THF, acetone, n-hexane, isooctane, and ionic liquid [ BMim ]][PF 6 ]And an ionic liquid [ BMIm][NTF 2 ]A mixed solvent composed of one of the above and a buffer solution. And preferably, the ionic liquid and the buffer solution are mixedA solvent, and a buffer solution may be prepared according to the preparation conditions of this example, and potassium phosphate buffer may be used, for example.
In a specific preparation, the concentration of 2-iodo-2-cyclohexenone added in the above step a may be 5 to 50mM, preferably 25mM. The molar ratio of the 2-iodo-2-cyclohexenone and the Pd catalyst added may be 1. The molar ratio of 2-iodo-2-cyclohexenone and base added can be 1.
In addition, the coupling reaction in step a may preferably be a mechanical stirring reaction at 70 ℃ for 6h.
The step b of preparing the tertiary α -aryl cyclic ketone in this embodiment specifically includes a mode one or a mode two, wherein, for the mode one, the mode is a two-step one-pot cascade reaction mode, and as shown in fig. 1, the method includes:
b11. b, when the reaction liquid in the step a is reduced to room temperature, adjusting the pH value of the reaction liquid to 6-8;
b12. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to ensure that the cells are suspended and dispersed again;
b13. adding NADPH and glucose into the reaction solution, and stirring at 25-35 ℃ for reaction for 6-18h;
b14. after the reaction is finished, extracting and drying are carried out, and after the extraction filtration and the desolventization, the tertiary alpha-aryl cyclic ketone in white solid is obtained by silica gel column chromatography.
The second mode is a two-step two-pot mode which is different from the first mode and is a one-pot two-step mode, and the mode specifically comprises the following steps:
b21. b, extracting the reaction liquid in the step a by using dichloromethane, drying by using anhydrous magnesium sulfate, and separating and purifying to obtain a generated intermediate product;
b22. dissolving the separated and purified intermediate product in a solvent to obtain a reaction solution;
b23. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to ensure that the cells are suspended and dispersed again;
b24. adding NADPH and glucose into the reaction solution, and stirring at 25-30 ℃ to react for 6-18h;
b25. after the reaction is finished, extracting and drying are carried out, and after the extraction filtration and the desolventization, the tertiary alpha-aryl cyclic ketone in white solid is obtained by silica gel column chromatography.
In both modes, it is preferable that the step b11 is to adjust the pH of the reaction solution to 7, and the steps b13 and b24 are to add NADPH and glucose and then to stir the reaction at 30 ℃ for 12 hours.
In addition, in the step b, after the freeze-dried powder containing the aged yellow enzyme and the glucose dehydrogenase whole cells is added, the cells can be re-suspended and dispersed by repeatedly blowing and beating the freeze-dried powder by using a pipette. In addition, the ratio of petroleum ether to ethyl acetate in the silica gel column is 10, and the step b14 and the step b25 are specifically extracted by dichloromethane after the reaction is finished, and dried by anhydrous magnesium sulfate.
Based on the above description of the overall design, the preparation of the tertiary alpha-aryl cyclic ketones of this example is further illustrated in the following specific examples.
Example 1
This example relates to the preparation of Pd catalyst, and example 1 specifically exemplifies 10% loading.
Dissolving 56mg of the prepared Magnetic Mesoporous Silica Nanoparticle (MMSN) in 10mL of deionized water, and performing ultrasonic dispersion for 20 min. 10mg of the Pd precursor NaPdCl are then added 4 Dissolved in 10mL of deionized water, added dropwise to the mixture obtained above, and stirred at 30 ℃ for 4 hours. Finally, 6.1mg of NaBH 4 Dissolved in 2mL of deionized water, added dropwise to the mixture and stirred at 30 ℃ for 2h. After the reaction is finished, pd @ MMSN-10 is obtained through magnetic separation.
SEM and TEM-Mapping charts of Pd @ MMSN-10 prepared in example 1 are shown in FIGS. 2 and 3, respectively, and f, g, h, i in FIG. 3 represent Si element distribution, O element distribution, fe element distribution and Pd element distribution, respectively.
Example 2
This example relates to the preparation of a tertiary alpha-aryl cyclic ketone based on the Pd catalyst prepared in example 1, and example 2 employs mode one above, which is a one-pot mode.
Adding 0.25mmol of 2-iodine-2-cyclohexane into a reaction vessel in sequenceKetene, 0.25mmol of phenylboronic acid derivative, 0.5mmol of potassium carbonate, 10mol of Pd @ MMSN-10,8mL of buffer solution and 2mL of ionic liquid [ BMIm][PF 6 ]And carrying out mechanical stirring reaction at 70 ℃ for 6 hours to carry out coupling reaction to obtain an intermediate product.
After the reaction is finished, the pH value of the reaction liquid system is adjusted to 7 after the temperature of the reaction liquid is reduced to room temperature. Then 0.2g of freeze-dried powder containing the aged yellow enzyme and glucose dehydrogenase whole cells is added into the system, and the mixed solution is repeatedly blown by a 5mL liquid transfer gun to resuspend and disperse the cells.
Finally, NADPH (0.2 mM) and glucose (0.2M) were added, and the reaction was stirred at 30 ℃ for 12 hours. After the reaction is finished, dichloromethane is used for extraction, anhydrous magnesium sulfate is used for drying, and after suction filtration and desolventization, white solid-shaped tertiary alpha-aryl cyclic ketone is obtained through silica gel column chromatography.
Example 3
This example relates to the preparation of a tertiary alpha-aryl cyclic ketone based on the Pd catalyst prepared in example 1, and example 2 employs mode two, which is a two-step, two-pot model as described above.
0.25mmol 2-iodine-2-cyclohexenone, 0.25mmol phenylboronic acid derivative, 0.5mmol potassium carbonate, 10mol Pd @ MMSN-10,8mL buffer solution and 2mL ionic liquid [ BMIm ] [ PF6] are sequentially added into a reaction vessel, and mechanical stirring reaction is carried out at 70 ℃ for 6 hours to carry out coupling reaction, so as to obtain an intermediate product.
After the reaction is finished, dichloromethane is used for extraction, anhydrous magnesium sulfate is used for drying, and the intermediate product is separated and purified.
The purified intermediate was dissolved in 8mL of buffer solution and 2mL of ionic liquid [ BMIm][PF 6 ]0.2g of freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase is added into the mixed solution, and the mixed solution is repeatedly blown by a 5mL pipette to resuspend and disperse the cells.
Finally, NADPH (0.2 mM) and glucose (0.2M) were added, and the reaction was stirred at 30 ℃ for 12 hours. After the reaction is finished, extracting with dichloromethane, drying with anhydrous magnesium sulfate, performing suction filtration and desolventizing, and performing silica gel column chromatography to obtain the white solid tertiary alpha-aryl cyclic ketone.
The conversion rate of the tertiary α -aryl cyclic ketone prepared in example 2 and example 3 was measured by nuclear magnetic resonance, the enantioselectivity of the compound was measured by liquid chromatography, and the nuclear magnetic resonance spectrum and the hplc data of the tertiary α -aryl cyclic ketone when different phenylboronic acid derivatives were used were measured as shown in the table below.
As can be seen from the above table, in the preparation method of the present embodiment, the effect of the mode one in the step b is significantly better than that of the mode two in yield, and a better ee value is obtained in some products, which fully illustrates that compared to the two-step two-pot mode of the mode two, the chemical-enzymatic method of the one-pot mode for preparing the tertiary α -aryl cyclic ketone can not only omit the complicated step of separating and purifying the intermediate product, but also reduce the loss of the intermediate product and the product, and has a better application effect, and is a preferred preparation mode.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.
Claims (7)
1. A process for preparing a tertiary α -aryl cyclic ketone, the process comprising:
a. an intermediate preparation step, and the intermediate preparation step comprises:
sequentially adding 2-iodine-2-cyclohexenone, a phenylboronic acid derivative, alkali, a Pd catalyst and a solvent into a reaction vessel, and stirring at 60-80 ℃ for coupling reaction for 4-12h to obtain a reaction solution with a generated intermediate product;
b. a tertiary alpha-aryl cyclic ketone preparation step, and the tertiary alpha-aryl cyclic ketone preparation step includes the following mode one or mode two, wherein:
the first mode comprises the following steps:
b11. b, when the reaction liquid in the step a is reduced to room temperature, adjusting the pH value of the reaction liquid to 6-8;
b12. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to ensure that the cells are suspended and dispersed again;
b13. adding NADPH and glucose into the reaction solution, and stirring at 25-35 ℃ for reaction for 6-18h;
b14. after the reaction is finished, extracting and drying, and after the extraction, the filtration and the desolventization, carrying out silica gel column chromatography to obtain the white solid tertiary alpha-aryl cyclic ketone;
the second mode includes:
b21. b, extracting the reaction liquid in the step a by using dichloromethane, drying by using anhydrous magnesium sulfate, and separating and purifying to obtain a generated intermediate product;
b22. dissolving the separated and purified intermediate product in a solvent to obtain a reaction solution;
b23. adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase into the reaction solution, and repeatedly blowing to ensure that the cells are suspended and dispersed again;
b24. adding NADPH and glucose into the reaction solution, and stirring at 25-30 ℃ to react for 6-18h;
b25. after the reaction is finished, extracting and drying, and after the extraction, the filtration and the desolventization, carrying out silica gel column chromatography to obtain the white solid tertiary alpha-aryl cyclic ketone;
the phenylboronic acid derivative is one of phenylboronic acid, 2-methylphenylboronic acid, 3-methylphenylboronic acid, 4-chlorophenylboronic acid, 2-methyl-4-chlorophenylboronic acid, 4-methoxyphenylboronic acid and 2-naphthylboronic acid;
the preparation of the Pd catalyst comprises the following steps:
c1. preparing an aminated modified magnetic mesoporous silica nanoparticle;
c2. dissolving magnetic mesoporous silica nanoparticles in deionized water, and performing ultrasonic dispersion to obtain a mixed solution;
c3. pd precursor NaPdCl 4 Dissolving in deionized water, dripping into the mixed solution, and stirring at 30 deg.C for reaction;
c4. reacting NaBH 4 Dissolving in deionized water, dripping into the mixed solution, and continuously stirring at 30 ℃ for reaction;
c5. after the reaction is finished, pd @ MMSN is obtained through magnetic separation;
the solvent is ionic liquid [ BMIm][PF 6 ]And a mixed solvent composed of the buffer solution.
2. The process according to claim 1 for the preparation of a tertiary alpha-aryl cyclic ketone, characterized in that: the alkali is alkali metal hydroxide or alkali metal carbonate.
3. The process of claim 1, wherein the tertiary alpha-aryl cyclic ketone comprises: in the step a, the concentration of the added 2-iodo-2-cyclohexenone is 5-50mM, the molar ratio of the added 2-iodo-2-cyclohexenone to the Pd catalyst is 1.
4. The process of claim 3, wherein the tertiary α -aryl cyclic ketone comprises:
in the step a, the concentration of the added 2-iodo-2-cyclohexenone is 25mM, the molar ratio of the added 2-iodo-2-cyclohexenone to the Pd catalyst is 1, the molar ratio of the added 2-iodo-2-cyclohexenone to the base is 1;
in step b, the pH of the reaction solution was adjusted to 7 in step b11, and the reaction was stirred at 30 ℃ for 12 hours after the addition of NADPH and glucose in steps b13 and b24.
5. The process according to claim 1 for the preparation of a tertiary alpha-aryl cyclic ketone, characterized in that: adding freeze-dried powder containing the whole cells of the old yellow enzyme and the glucose dehydrogenase, and repeatedly blowing and beating by using a pipette to re-suspend and disperse the cells.
6. The process according to claim 1 for the preparation of a tertiary alpha-aryl cyclic ketone, characterized in that: the ratio of petroleum ether to ethyl acetate in the silica gel column is 10.
7. The process according to claim 1 for the preparation of a tertiary alpha-aryl cyclic ketone, characterized in that: in the step b, the step b14 and the step b25 are extracted by dichloromethane after the reaction is finished, and dried by anhydrous magnesium sulfate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110190279.4A CN112877372B (en) | 2021-02-18 | 2021-02-18 | Process for preparing tertiary alpha-aryl cyclic ketones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110190279.4A CN112877372B (en) | 2021-02-18 | 2021-02-18 | Process for preparing tertiary alpha-aryl cyclic ketones |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112877372A CN112877372A (en) | 2021-06-01 |
CN112877372B true CN112877372B (en) | 2022-12-09 |
Family
ID=76057586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110190279.4A Active CN112877372B (en) | 2021-02-18 | 2021-02-18 | Process for preparing tertiary alpha-aryl cyclic ketones |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112877372B (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010075574A2 (en) * | 2008-12-25 | 2010-07-01 | Codexis, Inc. | Enone reductases |
CN102162002A (en) * | 2011-01-24 | 2011-08-24 | 浙江大学 | Method for synthesizing cyclohexanone derivatives by virtue of acylase-catalyzed multistep series connection |
CN102858987A (en) * | 2010-02-01 | 2013-01-02 | 巴斯夫欧洲公司 | Process for the reduction of cinnamaldehyde derivative employing enoate reductases |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103554183A (en) * | 2013-09-11 | 2014-02-05 | 南开大学 | Synthetic method and application of novel multi-aryl bridged long-chain diphosphine ligand |
CN105289725B (en) * | 2015-10-20 | 2017-10-10 | 华东师范大学 | A kind of preparation method and applications of quinine heterogeneous catalyst |
-
2021
- 2021-02-18 CN CN202110190279.4A patent/CN112877372B/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010075574A2 (en) * | 2008-12-25 | 2010-07-01 | Codexis, Inc. | Enone reductases |
CN102858987A (en) * | 2010-02-01 | 2013-01-02 | 巴斯夫欧洲公司 | Process for the reduction of cinnamaldehyde derivative employing enoate reductases |
CN102162002A (en) * | 2011-01-24 | 2011-08-24 | 浙江大学 | Method for synthesizing cyclohexanone derivatives by virtue of acylase-catalyzed multistep series connection |
Non-Patent Citations (1)
Title |
---|
Cooperative asymmetric reactions combining photocatalysis and enzymatic catalysis;Zachary C. Litman et al.;《Nature》;20180816;355-359 * |
Also Published As
Publication number | Publication date |
---|---|
CN112877372A (en) | 2021-06-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106520849B (en) | Method for preparing chiral 2-chloro-3, 4-difluorophenethyl alcohol | |
CN110452150B (en) | Axial chiral indole-naphthalene compound and preparation method thereof | |
CN113173900A (en) | Synthetic method of vitreous chromogen | |
CN112121853B (en) | Mesoporous hollow silica nanosphere loaded with prolinol catalyst as well as preparation method and application of mesoporous hollow silica nanosphere | |
CN103319311A (en) | Preparation method of crizotinib intermediate (1S)-1-(2, 6-dichloro-3-fluorophenyl)ethanol | |
CN105964306B (en) | It is a kind of based on poly ion liquid magnetic nano-particle, preparation method and its application in three component reactions | |
CN112877372B (en) | Process for preparing tertiary alpha-aryl cyclic ketones | |
CN102153500B (en) | Method for synthesizing diindolylmethane derivative | |
CN102766032B (en) | Oxidation method of cyclohexane | |
CN109897874A (en) | A method of preparing chiral isoquinolinecarboxylic acid | |
CN113527021A (en) | Preparation method of formamide compound | |
CN104711299B (en) | A kind of adrenergic preparation method | |
CN109369448A (en) | A kind of method that bimetal composite oxide catalyzes and synthesizes azobenzene compound | |
CN102190642A (en) | Preparation method and purification technique of dicyclic compound | |
CN113105321B (en) | Copper-based metal organic framework compound, preparation method and application thereof | |
CN111889144B (en) | Preparation method of chiral heteropolyacid loaded hollow mesoporous nano microsphere, product and application thereof | |
CN111849959B (en) | Method for preparing cycloastragaloside by using co-immobilized double-enzyme catalytic astragaloside IV | |
CN109851487B (en) | Method for preparing cyclocitral by selective cyclization of citral under catalysis of supported molybdenum carbide | |
CN111871458A (en) | Magnetic material supported chiral imidazolium salt catalyst and preparation method and application thereof | |
CN115925527B (en) | Method for preparing alpha-diaryl methyl substituted ketone compound | |
WO2023097691A1 (en) | Method for obtaining high-selectivity b-chiral branched-chain chiral amino acid | |
CN111732556B (en) | Deuterated loxapine medicine and preparation method thereof | |
CN111943924B (en) | Synthesis method of chromanone compounds | |
CN111718245B (en) | Method for preparing deuterated chemicals through photocatalytic decarboxylation conversion | |
CN106397117A (en) | Reduction alcoholization and resolution method of cyclohexyl phenyl ketone |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |