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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589182Generated: November 2, 2026

Tetrahydrofuran → 4-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

https://huagongshe.com/reaction/1589182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(Imidazole-1-yl)-propylamine DihydrochlorideHCID 12250969—
SolventWaterHCID 962—
Product4-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamideHCID 13588955—

Reaction Steps

A mixture of 1.54 g. of 4-fluorophenylacetic acid, 1.62 g. of 1,1'-carbonyldiimidazole and 30 ml. of tetrahydrofuran was stirred for 2 hours, then 1.98 g. of 1H-imidazole-1-propanamine dihydrochloride was added. Stirring was continued at room temperature for an additional 18 hours, then at reflux temperature for 5 hours, 5 ml. of water was added, the mixture was heated for 30 minutes and then concentrated to remove the volatile material. The residue was diluted with methylene chloride and 25 ml. of 1N sodium hydroxide and the layers separated. The organic layer was washed with water, dried over magnesium sulfate and concentrated, giving the desired product as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04568687
Source datasetuspto-grants-1986_02
ORD IDord-10943a0c07ab4282b49f50323488230c
Source noteuspto-grants-1986_02