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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075727Generated: November 1, 2026

Formaldehyde → 6-Chloro-1-ethyl-2-methyl-7-methylamino-5-trifluoromethylbenzimidazole

https://huagongshe.com/reaction/1075727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant6-Chloro-1-ethyl-2-methyl-5-(trifluoromethyl)-1H-benzimidazol-7-amineHCID 14281419—
Product6-Chloro-1-ethyl-2-methyl-7-methylamino-5-trifluoromethylbenzimidazoleHCID 2154060173.3%

Reaction Steps

To 1.0g. of 7-amino-6-chloro-1-ethyl-2-methyl-5-trifluoromethylbenzimidazole (Example IV) dissolved in 10 ml. of concentrated H2SO4 was added 1.0g. of paraformaldehyde. The resultant mixture was stirred at 80°C. for 2 hours and then poured onto ice. The resultant brown solution was made basic by addition of concentrated NH4OH, precipitating a light brown solid. The mixture was extracted with chloroform and the chloroform extracts washed with water and dried over Na2SO4. After removal of the chloroform by evaporation, the residue was extracted with hexane and the hexane extract distilled to dryness. The solid residue was recrystallized from hexane to give 0.77g. (73.3%) of the desired product, m.p. 116.5°-119°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954438
Source datasetuspto-grants-1976_05
ORD IDord-9fd6e9933156497cab8477bb0f19bbc1
Source noteuspto-grants-1976_05