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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439467Generated: November 1, 2026

Imidazole → alpha-Methyl-1H-imidazole-1-ethanol

https://huagongshe.com/reaction/1439467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantChloroacetoneHCID 6571—
SolventAcetonitrileHCID 6342—
Productalpha-Methyl-1H-imidazole-1-ethanolHCID 109233—

Reaction Steps

Chloroacetone (9.25 g.) in dry acetonitrile was added dropwise with stirring and ice cooling to a slurry of imidazole (13.6 g.) in acetonitrile (100 ml.). The mixture was stirred for 4 hours with ice cooling and then for 24 hours at room temperature. The solvent was removed and the product isolated by chromatography on silica gel, eluting with 10% methanol/dichloromethane. This material in 100 ml. of methanol was treated with excess sodium borohydride at 0° C. for 1 hour and acidified with methanolic hydrogen chloride. The solvent was removed, ethyl acetate added and the stirred mixture treated dropwise with saturated potassium carbonate solution until basic. The ethyl acetate was then decanted, dried, evaporated and the residue chromatographed on silica gel eluting with 10% methanol/dichloromethane to give pure 1-(2-hydroxypropyl)imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04059705
Source datasetuspto-grants-1977_11
ORD IDord-5f28a391f75a41de99a15c54236d2b5a
Source noteuspto-grants-1977_11