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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176664Generated: November 1, 2026

3,4-Difluoroaniline → HCID 11566903, compound

https://huagongshe.com/reaction/1176664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DifluoroanilineHCID 77469—
Reactant2-ChlorobenzimidazoleHCID 78572—
Reactant4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
SolventDiethyl ether methanolHCID 21864698—
ProductHCID 11566903HCID 11566903—

Reaction Steps

The title compound was prepared by Procedure B in two steps from 2-chloro-benzimidazole, 3,4-difluorobenzyl bromide and 3,4-difluoroaniline. The product was isolated by filtration and recrystallization (MeOH/Et2O) to give the title compound as its hydrochloride salt (white solid, mp 236-238° C.). MS(ES+) m/z 372 ([M+1]+, 100). 1NMR (DMSO-d6) δ 5.61 (s, 2H), 7.19-7.30 (m, 3H), 7.36-7.61 (m, 6H), 7.83-7.91 (m, 1H), 11.0 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842817B2
Source datasetuspto-grants-2010_11
ORD IDord-71cfb61a15a54ea48757649904051042
Source noteuspto-grants-2010_11