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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653175Generated: October 28, 2026

2-Aminothiophenol → 2-(Chloromethyl)benzothiazole

https://huagongshe.com/reaction/653175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantMethyl 2-chloroethanimidate--hydrogen chloride (1/1)HCID 12680765—
SolventDichloromethaneHCID 6344—
Product2-(Chloromethyl)benzothiazoleHCID 30497871.1%

Reaction Steps

To a solution of aminothiophenol (8.3 g) in methylene chloride at 0° C. is added methyl chloroacetimidate hydrochloride [prepared according to procedures described by R. Rogers and D. G. Nielson, Chem. Rev., 61, 179 (1961)](8.6 g). The reaction is allowed to warm to room temperature while stirring overnight. The mixture is washed with water three times; dried over magnesium sulfate and concentrated to an oil. The oil is distilled (120°-135° C. at 0.5 mm Hg) to give 7.8 g (71% yield) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675405
Source datasetuspto-grants-1987_06
ORD IDord-465ec160f50a4058b62cc6962c2f5f66
Source noteuspto-grants-1987_06