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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176668Generated: November 2, 2026

4-Chloro-3-(trifluoromethyl)aniline → HCID 11620357, compound

https://huagongshe.com/reaction/1176668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
Reactant2-ChlorobenzimidazoleHCID 78572—
Reactant4-Chloro-3-(trifluoromethyl)benzyl bromideHCID 2778114—
ProductHCID 11620357HCID 11620357—

Reaction Steps

The title compound was prepared by Procedure B in two steps from 2-chloro-benzimidazole, 4-chloro-3-trifluoromethylbenzyl bromide and 4-chloro-3-trifluoromethylaniline. The product was isolated by preparative LCMS to give the title compound as the free base (off-white solid, mp 88-92° C.). MS(ES+) m/z 504 (M+, 100). 1NMR (DMSO-d6) δ 5.60 (s, 2H), 7.02-7.15 (m, 2H), 7.25-7.32 (m, 2H), 7.45-7.52 (m, 1H), 7.63-7.70 (m, 2H), 7.81 (s, 1H), 8.23-8.40 (m, 2H), 9.62 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842817B2
Source datasetuspto-grants-2010_11
ORD IDord-0cbf4b7cf22a4318919bc6febc3eac1a
Source noteuspto-grants-2010_11