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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926479Generated: November 2, 2026

Benzimidazole → 2-(1H-Benzimidazol-1-yl)ethan-1-ol

https://huagongshe.com/reaction/1926479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantTetrahydrofuranHCID 8028—
ReactantIodoethanolHCID 12225—
ReactantSodium hydrideHCID 24758—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-(1H-Benzimidazol-1-yl)ethan-1-olHCID 228131—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a flask were added 2.3 g benzimidazole and 40 ml tetrahydrofuran and the mixture was cooled to 10 C under nitrogen. 1.0 g Sodium hydride were added in portions and the reaction mixture was stirred for 20 minutes. 4.0 g 2-Iodoethanol were added and the mixture was heated to 5° C. for 16 hours. The mixture was quenched slowly with 50 ml water, extracted twice with ethyl acetate and dried over sodium sulfate. Following filtration and solvent removal, the product was purified by silica gel chromatography using 25% methanol in ethyl acetate. A solid was obtained that was dissolved in a hot mixture of 10% methanol in ethyl acetate, cooled, filtered and dried giving 1.4 g white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08182718B2
Source datasetuspto-grants-2012_05
ORD IDord-f02daf4f822e4c4d983d9e2438a75702
Source noteuspto-grants-2012_05