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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926408Generated: October 25, 2026

2,5-Dichloro-1,3-benzothiazole → 2-Chloro-7-fluoro-4-trifluoromethyl-1,3-benzothiazole

https://huagongshe.com/reaction/1926408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichloro-1,3-benzothiazoleHCID 13314816—
Reactant2,3-Difluoro-6-(trifluoromethyl)anilineHCID 15614239—
ReactantHCID 178505734HCID 178505734—
Product2-Chloro-7-fluoro-4-trifluoromethyl-1,3-benzothiazoleHCID 67520773—

Reaction Conditions

Temperature90 °C

Reaction Steps

The title compound was prepared from 2,3-difluoro-6-trifluoromethylaniline via 2-mercapto-7-fluoro-4-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 90° C. for 4 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-92ed05d788bf43e0a77a50ac988de0b7
Source noteuspto-grants-2012_05