HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356819Generated: October 30, 2026
Acetate → (R)-2-(2,4-difluorophenyl)-3-isobutyryloxy-1,2-propanediol
https://huagongshe.com/reaction/356819
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetate | HCID 175 | — |
| Reactant | 1,3-Diisobutyryloxy-2-(2,4-difluorophenyl)-2-propanol | HCID 11290869 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | (R)-2-(2,4-difluorophenyl)-3-isobutyryloxy-1,2-propanediol | HCID 11150004 | 94.8% |
Reaction Steps
A 200 ml reaction vessel was charged with 2 g of 2-(2,4-difluorophenyl)-1,3-diisobutyryloxy-2-propanol, 100 mg of Lipase D made by Amano Pharmaceutical Co., Ltd. (derived from Rhizopus delemer, Enzyme No. 6), 90 ml of 50 mM acetate buffer (pH 5) and 10 ml of cyclohexane. The resulting mixture was stirred at 30° C. to react for 18 hours. After the reaction liquid was extracted three times with 50 ml of ethyl acetate, the organic layers were combined and the combined organic layer was washed with saturated aqueous solution with sodium bicarbonate and with saturated aqueous solution with sodium chloride and further dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by means of column chromatography on silica gel (eluent: n-hexane/ethyl acetate=3/2) to give 1.51 g of oily (R)-2-(2,4-difluorophenyl)-3-isobutyryloxy-1,2-propanediol. An optical purity thereof was determined in the same manner as Example 35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840553 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-34abcbff18c94a14ac90146106b5cd0e |
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| Source note | uspto-grants-1998_11 |
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