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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647801Generated: October 27, 2026

Cyclopropanecarbonyl chloride → 3-(p-Cyclopropylcarbonylaminobenzoyl)-propionic acid

https://huagongshe.com/reaction/647801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactant4-(4-Aminophenyl)-4-oxobutanoic acidHCID 243290—
SolventTetrahydrofuranHCID 8028—
Product3-(p-Cyclopropylcarbonylaminobenzoyl)-propionic acidHCID 2048337675.4%

Reaction Steps

3.2 g (30.6 millimoles) of cyclopropanecarboxylic acid chloride, dissolved in 20 ml of absolute tetrahydrofuran, are added dropwise, at room temperature, to a stirred solution of 5.0 g (25.9 millimoles) of 3-(p-aminobenzoyl)-propionic acid in 100 ml of absolute tetrahydrofuran; a precipitate forms. The reaction mixture is then kept for 7 hours under reflux. The product is filtered off at 10° C., washed with water and dried under reduced pressure at 50° C. 5.1 g (75% of theory) of 3-(p-cyclopropylcarbonylaminobenzoyl)-propionic acid are obtained as yellow crystals, of melting point 229°-230° C. (after recrystallization from ethanol/water).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410529
Source datasetuspto-grants-1983_10
ORD IDord-b104b6f4303643c3adab0bfd71c1569e
Source noteuspto-grants-1983_10