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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253346Generated: November 2, 2026

2-Aminothiophenol → 2-(Chloromethyl)benzothiazole

https://huagongshe.com/reaction/1253346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
Reactant2-Chloro-1,1,1-triethoxyethaneHCID 305922—
SolventDichloromethaneHCID 6344—
Product2-(Chloromethyl)benzothiazoleHCID 30497891.3%

Reaction Steps

A solution of 2-chloro-1,1,1-triethoxyethane (5.9 g) and 2-aminothiophenol (2.5 g) was heated at 80° C. for 15 minutes. After cooling to room temperature, it was dissovled in methylene chloride (30 ml) and the resulting solution was washed with 3N HCl (10 ml) and then with water (20 ml). The organic portion was evaporated and the residue chromatographed over silica gel to obtain 2-chloromethylbenzothiazole (3.35 g; 90% yield), m.p. 34° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748280
Source datasetuspto-grants-1988_05
ORD IDord-b50bfa9644894d42945dce4dca34c6ea
Source noteuspto-grants-1988_05