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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090116Generated: November 1, 2026

Thionyl Chloride → 1-(4-Fluorophenyl)-4-methyl-5-chloromethyl-1,2,3-triazole

https://huagongshe.com/reaction/1090116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanolHCID 19914681—
SolventBenzeneHCID 241—
Product1-(4-Fluorophenyl)-4-methyl-5-chloromethyl-1,2,3-triazoleHCID 19914675—

Reaction Steps

A solution of 1-(4-fluorophenyl)-4-methyl-5-hydroxymethyl-1,2,3-triazole (871 mg; 4.20 mmol), prepared as described in example 6, and thionyl chloride (400 ml; 5.46 mmol) in benzene (14 ml) was heated under reflux for 4 hours. The reaction mixture was kept under stirring at room temperature overnight, thionyl chloride and benzene were evaporated and the resultant crude compound was collected several times with benzene. After evaporation of the solvent, the crude compound was purified by chromatography on silica gel (230-400 mesh), eluent methylene chloride:acetone=95:5, giving the title compound (m.p. 70°-71° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081136
Source datasetuspto-grants-1992_01
ORD IDord-dce0ef16f7bd487a8ff610c1e8344581
Source noteuspto-grants-1992_01