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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699633Generated: November 2, 2026

1-(Bromomethyl)-4-(trifluoromethyl)benzene → HCID 18681029, compound

https://huagongshe.com/reaction/1699633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
ReactantPotassium BicarbonateHCID 516893—
ReactantN-benzenesulfonyl-4-acetylamino-3-aminobenzamideHCID 18680999—
SolventMethanolHCID 887—
ProductHCID 18681029HCID 1868102940.7%

Reaction Steps

A methanol (7 ml) solution of N-benzenesulfonyl-4-acetylamino-3-aminobenzamide (0.50 g), 4-(trifluoromethyl)benzyl bromide (0.418 g) and potassium bicarbonate (0.423 g) is stirred for 1 hour at 60° C. to give preliminarily purified N-benzenesulfonyl-4-acetylamino-3-[4-(trifluoromethyl)benzylamino]benzamide (0.30 g). This is dissolved in methanol. When it is left undisturbed crystals precipitated. The crystals are separated through filtration, dried and thus, 6-benzenesulfonylcarbamoyl-2-methyl-1-[4-(trifluoromethyl)benzyl]benzimidazole (0.160 g)is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348032B1
Source datasetuspto-grants-2002_02
ORD IDord-646eae58c74c434ea18a69879738848e
Source noteuspto-grants-2002_02