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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278897Generated: October 25, 2026

Chloroacetyl chloride → HCID 18623236, compound

https://huagongshe.com/reaction/278897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-2-(3,4-difluorophenyl)ethanolHCID 22048878—
SolventDichloromethaneHCID 6344—
ProductHCID 18623236HCID 18623236—

Reaction Steps

To a solution of 2-amino-2-(3,4-difluorophenyl)-ethanol 2.6 g, 15.0 mmol) in CH2Cl2 (15 mL) and 20% (by wt.) NaOH (15 mL) was added a solution of chloroacetyl chloride (1.32 mL, 16.5 mmol) in 15 mL of CH2Cl2 at −10° C. dropwise under argon atmosphere. After the addition was complete, the reaction mixture was stirred for 15 min and then it was transferred to a separatory funnel. The organic layer was separated and the aqueous layer was extracted with CH2Cl2 (2×20 mL). The combined organic extracts were washed with a solution containing 10 mL of brine and 5 drops of concentrated HCl. The organic layer was dried over MgSO4, filtered and the solvent was removed in vacuo to give a white solid. It was further purified with flash column chromatography on silica gel with 1:1 hexane/EtOAc followed by EtOAc as the eluting system. 2-Chloro-N-[1-(3,4-difluoro-phenyl)-2-hydroxy-ethyl]-acetamide was obtained as a white solid (2.6 g, 69.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362182B1
Source datasetuspto-grants-2002_03
ORD IDord-a284c40a06ed496f8cd76a8a475c1db2
Source noteuspto-grants-2002_03