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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946902Generated: October 31, 2026

Chloroacetyl chloride → N-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamide

https://huagongshe.com/reaction/1946902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-(3-bromophenyl)propan-1-olHCID 53256694—
SolventAcetonitrileHCID 6342—
ProductN-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamideHCID 5815528487.2%

Reaction Steps

A solution of crude (RS)-2-amino-2-(3-bromo-phenyl)-propan-1-ol (8.38 g, 36 mmol) and triethylamine (6.08 ml, 44 mmol) in acetonitrile (140 ml) was treated dropwise at −2° C. with chloro-acetyl chloride (3.25 ml, 40 mmol). After complete addition, the orange colored solution was left to warm to room temperature and stirring was continued for 2 h. For the workup, to the reaction was added silica gel (10 g) and it was evaporated at reduced pressure, thereafter, it was purified by chromatography on silica gel using a gradient of dichloromethane/methanol=100/0 to 90/10 as the eluent. There were obtained 9.62 g (86% of theory) of (RS)—N-[1-(3-bromo-phenyl)-2-hydroxy-1-methyl-ethyl]-2-chloro-acetamide as a light brown oil. MS (ISP): m/z=304.1 [M+H]+, 306.1 [M+2+H]+, 308.2 [M+4+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399459B2
Source datasetuspto-grants-2013_03
ORD IDord-1f06a2306cce4713820db28917993c36
Source noteuspto-grants-2013_03