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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731008Generated: October 25, 2026

Water → 1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diol

https://huagongshe.com/reaction/731008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant(3R)-1-Chloro-3-[(trimethylsilyl)oxy]butan-2-oneHCID 71415957—
ReactantHCID 178505836HCID 178505836—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diolHCID 23117040—

Reaction Steps

A solution of 0.7 g (3.6 mmol) of (R)-1-chloro-3-(trimethylsilyloxy)butan-2-one in 5 mL of THF was cooled to 0° C., 5.4 mL (3.8 mmol) of a 0.7 M solution of 2,4-difluorophenylmagnesium bromide prepared by the same method as that in Example 3 was added dropwise thereto over a period of 10 minutes. After the completion of the dropwise addition, stirring was continued for another 5 hours, and 10 mL of a saturated aqueous solution of ammonium chloride was added to stop the reaction. Furthermore, 10 mL of water was added, and extraction was performed with ethyl acetate (20 mL×2). After drying over anhydrous sodium sulfate, concentration was performed under reduced pressure to obtain 1-chloro-2-(2,4-difluorophenyl)butane-2,3-diol. A quantitative analysis was performed by HPLC (under the same HPLC measurement conditions as those in Example 6). As a result, the yield was determined to be 87% ((2S,3R)/(2R,3R)=41/59).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582781B2
Source datasetuspto-grants-2009_09
ORD IDord-a60c73777d054bffbe5b7debb14e95ad
Source noteuspto-grants-2009_09