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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517646Generated: November 3, 2026

Imidazole → (S)-Imidazol-1-YL-(tetrahydrofuran-2-YL)-methanone

https://huagongshe.com/reaction/1517646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant(S)-tetrahydrofuran-2-carbonyl chlorideHCID 42131216—
SolventChloroformHCID 6212—
Product(S)-Imidazol-1-YL-(tetrahydrofuran-2-YL)-methanoneHCID 57741232—

Reaction Conditions

Temperature0 °C

Reaction Steps

21.8 g (32.0 mmol) imidazole are placed in 400 ml chloroform and cooled to 0° C. 21.5 g (15.0 mmol) (S)-tetrahydrofuran-2-carbonyl chloride are added dropwise, then stirred for 1.5 hours at ambient temperature. After cooling again to 0° C. the reaction mixture is extracted with semisaturated sodium chloride solution. The organic phase is dried and evaporated to dryness. Yield: 23.5 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232286B2
Source datasetuspto-grants-2012_07
ORD IDord-85cc9b530a604b86a74f8f2a157213c9
Source noteuspto-grants-2012_07