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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606278Generated: November 3, 2026

Thionyl Chloride → 2-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzene

https://huagongshe.com/reaction/1606278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21444217HCID 21444217—
CatalystPyridineHCID 1049—
Product2-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzeneHCID 21444251—

Reaction Steps

β,β-Dichloro-α-(3-chloro-4-cyclohexylphenyl)ethanol (67.5 g.; 0.22 moles) is heated with thionyl chloride (110 ml) containing 1 drop of pyridine until solution is obtained. The heating is discontinued and the reaction is allowed to proceed at room temperature for 12 hours. The reaction mixture is heated for an additional hour and the thionyl chloride removed, chased by benzene several times and distilled to give β,β,α,3-tetrachloro-4-cyclohexylphenylethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952067
Source datasetuspto-grants-1976_04
ORD IDord-a493121916cf43fd8c6c579dc608070d
Source noteuspto-grants-1976_04