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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060508Generated: October 31, 2026

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

https://huagongshe.com/reaction/1060508

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 numberUS06524552B2
Source datasetuspto-grants-2003_02
ORD IDord-a8a3c381a53a47d5a21ebe2828a2b33b
Source noteuspto-grants-2003_02