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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576992Generated: October 25, 2026

Ammonium Chloride → (1-methyl-1H-1,3-benzodiazol-2-yl)methanol

https://huagongshe.com/reaction/576992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-methyl-1H-1,3-benzodiazole-2-carbaldehydeHCID 762084—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(1-methyl-1H-1,3-benzodiazol-2-yl)methanolHCID 34417799%

Reaction Steps

To a 0° C. solution of 1-methyl-1H-benzimidazole-2-carbaldehyde (1.1 g, 6.8 mmol) in anhydrous methanol (50 mL) was added sodium borohydride (350 mg, 9.3 mmol). The reaction mixture was stirred at room temperature for 5 hours. Saturated ammonium chloride solution (20 mL) was added. Methanol was evaporated. The resultant mixture was extracted with EtOAc (3×50 mL) and CH2Cl2 (1×50 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo. (1-methyl-1H-benzimidazol-2-yl)methanol was obtained (1.1 g, 99% yield). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-b23eeefdeb0146999159da3c67bbdb90
Source noteuspto-grants-2015_05