Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731012Generated: October 30, 2026

Water → 1-Chloro-2-(2,4-difluorophenyl)-3-pivaloyloxybutan-2-ol

https://huagongshe.com/reaction/731012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86606435HCID 86606435—
ReactantHCID 178505836HCID 178505836—
SolventTolueneHCID 1140—
Product1-Chloro-2-(2,4-difluorophenyl)-3-pivaloyloxybutan-2-olHCID 2311704171%

Reaction Steps

A solution of 0.41 g (2.0 mmol) of (R)-1-chloro-3-pivaloyloxybutan-2-one in 5 mL of toluene was cooled to 0° C., and 3.2 mL (2.2 mmol) of a 0.69 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 5 minutes. After the completion of the dropwise addition, stirring was continued for another 1 hour, 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 0.54 g of a crude product. The resulting product was purified by column on silica gel to obtain 0.450 g of the title compound (yield: 71%) ((2S,3R)/(2R,3R)=93/7 (the diastereomeric ratio was measured by HPLC under the same HPLC measurement conditions as those in Example 19)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582781B2
Source datasetuspto-grants-2009_09
ORD IDord-8cb5a24fe6e1424bb23bb4d01262e7b5
Source noteuspto-grants-2009_09