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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731013Generated: October 30, 2026

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

https://huagongshe.com/reaction/731013

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 2311704194%

Reaction Conditions

Temperature0 °C

Reaction Steps

First, 8.9 mL (8.0 mmol) of a 0.9 M solution of 2,4-difluorophenylmagnesium bromide prepared by the same method as that in Example 3 was cooled to 0° C., and a solution of 0.83 g (4.0 mmol) of (R)-1-chloro-3-pivaloyloxybutan-2-one in 10 mL of toluene 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 20 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 (30 mL×2). After drying over anhydrous sodium sulfate, concentration was performed under reduced pressure to obtain 1.57 g of a crude product. A quantitative analysis was performed by HPLC. Thereby, the title compound was obtained in a yield of 94% ((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-533ec3b654de4d8fa2a3daa7a17c3682
Source noteuspto-grants-2009_09