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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731001Generated: October 30, 2026

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

https://huagongshe.com/reaction/731001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium FluorideHCID 522689—
Reactant1-Chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-olHCID 23117047—
SolventMethanolHCID 887—
Product1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diolHCID 2311704017%

Reaction Steps

To a solution of 0.27 g (0.77 mmol) of 1-chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol ((2S,3R)/(2R,3R)=91/9) in 3 mL of methanol was added 0.06 g (0.94 mmol) of potassium fluoride, and reaction was performed for 10 hours and then at 50° C. for another 25 hours. Next, 5 mL of water was added to stop the reaction, and extraction was performed with 10 mL of ethyl acetate. The resulting organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product as a colorless oil. The resulting crude product was quantitatively analyzed by HPLC (under the same HPLC measurement conditions as those in Example 6). Thereby, the title compound was obtained in a yield of 17% ((2S,3R)/(2R,3R)=95/5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582781B2
Source datasetuspto-grants-2009_09
ORD IDord-a125feee18d0457d957eda867789655c
Source noteuspto-grants-2009_09