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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833851Generated: November 3, 2026

Thionyl Chloride → 1-(1-Chloroethyl)-2-fluorobenzene

https://huagongshe.com/reaction/1833851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Fluoro-alpha-methylbenzenemethanolHCID 123066—
SolventChloroformHCID 6212—
Product1-(1-Chloroethyl)-2-fluorobenzeneHCID 13564325—

Reaction Steps

Thionyl chloride (100 ml.) was added to a solution of 1-(2-fluorophenyl)ethanol [described by McCall, J.A.C.S. 74, 4809 (1952)] (105 g.) in dry chloroform (200 ml.). After the vigorous initial reaction had subsided, the solution was heated at reflux on a steam bath for 30 minutes. The excess of thionyl chloride was removed by repeated co-distillation with dry toluene and the residue was diluted with diethyl ether, washed with water (2 × 100 ml.), dried over sodium sulphate, filtered and evaporated to a yellow liquid, which was distilled to give 1-(2-fluorophenyl)ethyl chloride (73.2 g.), b.p. 70°-75° C./20 mm.Hg, as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067723
Source datasetuspto-grants-1978_01
ORD IDord-97e5ae75f6dc4ff9b4ec9afd062596c0
Source noteuspto-grants-1978_01