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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276035Generated: October 26, 2026

Sodium Sulfate → 1h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl-

https://huagongshe.com/reaction/276035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
Reactant1-(2-Chlorobenzyl)-6-ethoxycarbonyl-2-methylbenzimidazoleHCID 18680839—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantLithium ammonium hydrideHCID 86650320—
SolventTetrahydrofuranHCID 8028—
Product1h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl-HCID 1831553862.5%

Reaction Steps

A solution of 2.66 g of 1-(2-chlorobenzyl)-6-ethoxycarbonyl-2-methylbenzimidazole in 20 ml of tetrahydrofuran was slowly added to a solution of 1.54 g of lithium aluminum hydride in 20 ml of tetrahydrofuran at a temperature of from 20 to 25° C. Further, the mixture was stirred at room temperature for 1 hour. Thirty milliliters of tetrahydrofuran were added thereto to dilute the reaction solution. Lithium ammonium hydride was decomposed and solidified with a saturated aqueous solution of sodium sulfate, and the tetrahydrofuran layer was separated. The solvent was distilled off, and the residue was purified through silica-gel column chromatography (eluent: a mixture of chloroform and methanol at a ratio of 9:1) to give 1.45 g of 1-(2-chlorobenzyl)-6-hydroxymethyl-2-methylbenzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-b9780ffbde374e5eafda12e93553ae47
Source noteuspto-grants-2002_03