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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647808Generated: October 25, 2026

4-(4-Aminophenyl)-4-oxobutanoic acid → 3-[p-(1-Chlorocyclopropylcarbonylamino)-benzoyl]-propionic acid

https://huagongshe.com/reaction/647808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Aminophenyl)-4-oxobutanoic acidHCID 243290—
ReactantCyclopropanecarbonyl chloride, 1-chloro-HCID 10942508—
SolventTetrahydrofuranHCID 8028—
Product3-[p-(1-Chlorocyclopropylcarbonylamino)-benzoyl]-propionic acidHCID 2048337149.3%

Reaction Steps

3.9 g (28.1 millimoles) of 1-chlorocyclopropanecarboxylic acid chloride are added, with stirring, to 4.5 g (23.3 millimoles) of 3-(p-aminobenzoyl)-propionic acid in 100 ml of absolute tetrahydrofuran. The reaction mixture is then stirred for 20 hours at room temperature, followed by 7 hours under reflux. A small amount of solid is filtered off and discarded, and the filtrate is concentrated. The residue obtained is recrystallized from ethyl acetate, giving 3.4 g (49% of theory) of 3-[p-(1-chlorocyclopropylcarbonylamino)-benzoyl]-propionic acid as colorless crystals, of melting point 178°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410529
Source datasetuspto-grants-1983_10
ORD IDord-74d38cc0253c41d886bfa8b64df79659
Source noteuspto-grants-1983_10