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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723110Generated: November 1, 2026

Tetrahydrofuran → (2-Methyl-1H-benzimidazol-4-yl)methanol

https://huagongshe.com/reaction/1723110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantLithium aluminum hydrideHCID 28112—
Reactantethyl 2-methyl-1H-benzimidazole-4-carboxylateHCID 18680979—
SolventWaterHCID 962—
Product(2-Methyl-1H-benzimidazol-4-yl)methanolHCID 2002666479.4%

Reaction Steps

(a-2) A cooled (0° C.) solution of 10 parts of ethyl 2-methyl-1H-benzimidazole-4-carboxylate in 45 parts of tetrahydrofuran was added dropwise to a suspension of 4 parts of lithium tetrahydroaluminate in 45 parts of tetrahydrofuran. Upon complete addition, the temperature was allowed to reach room temperature. After the addition of ethyl acetate and water, the reaction mixture was filtered over diatomaceous earth. The filtrate was evaporated, yielding 6.3 parts (79.4%) of 2-methyl-1H-benzimidazole-4-methanol as a residue (int. 66).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859684
Source datasetuspto-grants-1989_08
ORD IDord-fdcb98520d294504a9287656ca2d82b5
Source noteuspto-grants-1989_08