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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285734Generated: November 1, 2026

Acetonitrile → HCID 178491309, compound

https://huagongshe.com/reaction/2285734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant1-BenzylimidazoleHCID 77918—
ProductHCID 178491309HCID 178491309—

Reaction Steps

Anisoyl chloride (4.3 ml) was added slowly to a stirred solution of 1-benzylimidazole (5.0 g) in dry acetonitrile (50 ml) keeping the temperature at 25°-30°. After stirring for 1 h. triethylamine (4.4 ml) was added dropwise and the mixture stirred for 18 h. then filtered. The filtrate was concentrated to dryness, and the residue taken up into ether (100 ml) and washed with acetic acid (25%, 3×50 ml), and 2 N sodium carbonate (3×50 ml), then concentrated until the title compound crystallised as a white solid, m.p. 108°-110° (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04324792
Source datasetuspto-grants-1982_04
ORD IDord-71747a5102304c7da6568401b47aa5ae
Source noteuspto-grants-1982_04