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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
Reactant1,3-Diisobutyryloxy-2-(2,4-difluorophenyl)-2-propanolHCID 11290869—
SolventCyclohexaneHCID 8078—
Product(R)-2-(2,4-difluorophenyl)-3-isobutyryloxy-1,2-propanediolHCID 1115000494.8%

Reaction Conditions

Temperature30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840553
Source datasetuspto-grants-1998_11
ORD IDord-34abcbff18c94a14ac90146106b5cd0e
Source noteuspto-grants-1998_11