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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46720Generated: October 25, 2026

Benzaldehyde → 7-Benzylidenamino-1-ethyl-2-methyl-5-trifluoromethyl-6-chlorobenzimidazole

https://huagongshe.com/reaction/46720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzenesulfonic AcidHCID 7371—
Reactant6-Chloro-1-ethyl-2-methyl-5-(trifluoromethyl)-1H-benzimidazol-7-amineHCID 14281419—
SolventO-XyleneHCID 7237—
Product7-Benzylidenamino-1-ethyl-2-methyl-5-trifluoromethyl-6-chlorobenzimidazoleHCID 2038538194%

Reaction Steps

Benzaldehyde (0.78 g.; 7.35 mmole) was reacted with 1-ethyl-2-methyl-5-trifluoromethyl-6-chloro-7-aminobenzimidazole (1.0 g.; 3.66 mmole) in the presence of 7 ml. of xylene and a few crystals of benzenesulfonic acid. The mixture was refluxed for 1 hour, removing water from the reaction mixture. Upon cooling to room temperature, the product crystallized out of solution to give 1.24 g. (94% yield). After recrystallization from benzene, the product melts at 183°-185.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174959
Source datasetuspto-grants-1979_11
ORD IDord-dee3b648626c42eaa7460360357e10a3
Source noteuspto-grants-1979_11