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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613278Generated: October 27, 2026

Thionyl Chloride → N-(4-chloro-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide

https://huagongshe.com/reaction/1613278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantN-(4-hydroxy-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamideHCID 15023453—
CatalystDimethylformamideHCID 6228—
SolventChloroformHCID 6212—
ProductN-(4-chloro-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamideHCID 15023451—

Reaction Steps

Thionyl chloride (4.8 ml) was added dropwise to a mixture of N-(4-hydroxy-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide (6.56 g) and N,N-dimethylformamide (5 drops) in dry chloroform (145 ml) at 0° C. and the reaction mixture was refluxed for 1 hour. The mixture was washed successively with water, 1N aqueous sodium hydroxide solution, and sodium chloride, aqueous solution, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel with a mixture of n-hexane and ethyl acetate (5:1) as an eluent to give N-(4-chloro-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide as white powder (6.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192779
Source datasetuspto-grants-1993_03
ORD IDord-2bfb5e5c00994a42b744ecc46c8a37a8
Source noteuspto-grants-1993_03