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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397489Generated: October 26, 2026

Diisobutylaluminum hydride → 5-(Hydroxymethyl)-1H-benzimidazole

https://huagongshe.com/reaction/397489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl 1H-benzimidazole-6-carboxylateHCID 13505555—
SolventDichloromethaneHCID 6344—
Product5-(Hydroxymethyl)-1H-benzimidazoleHCID 13505556—

Reaction Steps

To a cooled (0° C.) suspension of ethyl-benzimidazole-5-carboxylate (4.76 g, 25 mmol) in CH2Cl2 (100 mL) was added a 1 M solution of DIBAL in CH2Cl2 (100 mL) and the mixture was stirred for 4 h. The reaction was quenched by the sequential addition of MeOH (8 mL), 1M NaOH (16 mL), and 30% sodium potassium tartrate (40 mL). The mixture was warmed to RT and filtered, and the solid residue was washed with CH2Cl2. The filtrate was concentrated in vacuo to afford the title compound as a brown solid: 1H NMR (400 MHz, DMSO-d6): δ4.58 (s, 1H), 7.14 (m, 1H), 7.46 (s, 1H), 7.51 (m, 1H), 8.15 (s, 1H); HRMS (FAB) C8H9N2O calcd. 149.1723 (M+1). Found 149.1045.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610701B2
Source datasetuspto-grants-2003_08
ORD IDord-2b7aeb2f4d7f40889c0149c021f90d69
Source noteuspto-grants-2003_08