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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350587Generated: October 30, 2026

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

https://huagongshe.com/reaction/350587

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 numberUS07182934B2
Source datasetuspto-grants-2007_02
ORD IDord-f8bde9eff2d24d42912c29510dd56676
Source noteuspto-grants-2007_02