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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896945Generated: October 29, 2026

Sodium borohydride → (1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazol-5-yl)methanol

https://huagongshe.com/reaction/896945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazole-5-carbaldehydeHCID 15088505—
SolventMethanolHCID 887—
Product(1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazol-5-yl)methanolHCID 15088539—

Reaction Steps

Sodium borohydride (1.1 g, 29 mmole) was added in three portions to a stirred mixture of crude 1-benzyl-4-chloro-5-formyl-2-(4-nitrophenyl)imidazole (54.2 g, 88 mmole) in methanol (250 ml) at room temperature. After two hours, more sodium borohydride (0.51 g, 15 mmol) was added, the mixture was stirred for 30 minutes and the methanol was evaporated. The residue was mixed with water (250 ml) and extracted with methylene chloride (200 ml, 3×50 ml). The combined organic solutions were washed with water (2×50 ml) and dried (NaSO4) overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921525B2
Source datasetuspto-grants-2005_07
ORD IDord-e686edc2b26845369706b226ea9640f9
Source noteuspto-grants-2005_07