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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926392Generated: November 2, 2026

2-Fluoro-5-(trifluoromethyl)aniline → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/1926392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-(trifluoromethyl)anilineHCID 136349—
Reactant2,5-Dichloro-1,3-benzothiazoleHCID 13314816—
Reactant5-(trifluoromethyl)-1,3-benzothiazole-2-thiolHCID 178419087—
Product2-Chloro-5-(trifluoromethyl)-1,3-benzothiazoleHCID 21985849—

Reaction Conditions

Temperature95 °C

Reaction Steps

The title compound was prepared from 2-fluoro-5-trifluoromethylaniline via 2-mercapto-5-trifluoromethyl-1,3-benzothiazole as described for 2,5-dichloro-1,3-benzothiazole except that in the first step the reaction mixture was heated to 95° C. for 4 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-cb179b5601b245b6b12255b4d7b86bd6
Source noteuspto-grants-2012_05