Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442416Generated: October 27, 2026

Hydrochloric Acid → 4-(2-Carboxyethyl)benzalacetophenone

https://huagongshe.com/reaction/442416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantAcetophenoneHCID 7410—
Reactant3-(4-Formylphenyl)propanoic acidHCID 19825241—
SolventSodium HydroxideHCID 14798—
Product4-(2-Carboxyethyl)benzalacetophenoneHCID 54386652100%

Reaction Steps

To a solution of 5.34 g of 4-formyldihydrocinnamic acid in 50 ml of 1N sodium hydroxide was added a solution of 3.6 g of acetophenone and 20 ml of ethanol. The reaction mixture was stirred at room temperature for 4 hrs. and then poured onto 300 g of crushed ice. 1N Hydrochloric acid was added and, after stirring at 0° C for 15 min., the precipitate was collected and washed with water. The precipitate was dissolved in 500 ml of ethyl acetate, dried over anhydrous sodium sulfate and the drying agent was collected on a filter. The filtrate was concentrated to about 100 ml and seeded with crystalline product. The solid was collected, washed with 1:4-ethyl acetate-ether followed by ether and dried at 70°-75° C under vacuum to give 8.4 g (72%) of 4-(2-carboxyethyl)benzalacetophenone, as yellow needles, m.p. 159°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045487
Source datasetuspto-grants-1977_08
ORD IDord-b6245513e4a643218c65df3c2ee2b63f
Source noteuspto-grants-1977_08