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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643006Generated: November 2, 2026

Sodium borohydride → (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol

https://huagongshe.com/reaction/643006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(5-bromopyridin-2-yl)-1H-imidazole-4-carbaldehydeHCID 86614005—
SolventMethanolHCID 887—
Product(1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanolHCID 6851193170.6%

Reaction Steps

To a suspension of 1-(5-bromopyridin-2-yl)-1H-imidazole-4-carbaldehyde (730 mg, 2.90 mmol) in MeOH (10 mL) at room temperature was added NaBH4 (134 mg, 3.53 mmol). The mixture was stirred for 30 min, during which time the suspension became clear. The solvent was removed in vacuo. The residue was partitioned between H2O and EtOAc. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol as a solid (520 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696352B2
Source datasetuspto-grants-2010_04
ORD IDord-7e810aad404940188a7f1a0bc6802032
Source noteuspto-grants-2010_04