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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52888Generated: October 29, 2026

Hydrochloric Acid → 1-[(2'-t-Butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-5-cyano-4-(alpha-hydroxybenzyl)imidazole

https://huagongshe.com/reaction/52888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Benzoyl-1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-5-cyanoimidazoleHCID 19036088—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product1-[(2'-t-Butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-5-cyano-4-(alpha-hydroxybenzyl)imidazoleHCID 1903617784.9%

Reaction Steps

50.5 mg of sodium borohydride were added to a solution of 691 mg of 4-benzoyl-1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-5-cyanoimidazole [prepared as described in step (a) above] in 10 ml of ethanol, and the resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was then neutralized with aqueous hydrochloric acid, after which it was mixed with ethyl acetate and with a saturated aqueous solution of sodium chloride. The ethyl acetate layer was separated, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 589 mg of the title compound as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616599
Source datasetuspto-grants-1997_04
ORD IDord-38991e6f6bda47a7a36af5cb8fd7a748
Source noteuspto-grants-1997_04