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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328173Generated: October 30, 2026

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

https://huagongshe.com/reaction/328173

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 numberUS04016214
Source datasetuspto-grants-1977_04
ORD IDord-1b1b38b352c649f697b1fab4b6c5226b
Source noteuspto-grants-1977_04