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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644538Generated: October 30, 2026

Sodium borohydride → HCID 11372470, compound

https://huagongshe.com/reaction/644538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant7-(3-Acetylphenyl)-1-phenyl-5-trifluoromethylbenzimidazoleHCID 11428935—
SolventEthanolHCID 702—
ProductHCID 11372470HCID 11372470—

Reaction Steps

To a suspension of 7-(3-acetylphenyl)-1-phenyl-5-trifluoromethylbenzimidazole (0.95 g, 2.5 mmol) in ethanol (10 ml) was added sodium borohydride (0.1 g, 2.6 mmol) and the resultant mixture was stirred at 60° C. for 20 min. The cooled reaction mixture was concentrated under reduced pressure and the concentrate was partitioned between ethyl acetate and water. The organic layer was dried over magnesium sulphate and concentrated to a small volume (1-2 ml) under reduced pressure. The title product precipitated upon addition of ligroin to the concentrate (0.65 g, 68%) m/z, 383.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700638B2
Source datasetuspto-grants-2010_04
ORD IDord-239daf1ea2b144a9995990f6769d72fe
Source noteuspto-grants-2010_04