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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397664Generated: October 29, 2026

P-Chloroacetophenone → Ethyl 3-(4-chlorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/2397664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ChloroacetophenoneHCID 7467—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
ProductEthyl 3-(4-chlorophenyl)-3-oxopropanoateHCID 101336—

Reaction Steps

The starting material is prepared as follows: A solution of 96.6 g of 4-chloro acetophenone in 300 ml of diethyl carbonate is added dropwise to a suspension of 34 g sodium hydride (55% in mineral oil, washed twice with diethyl ether) in 400 ml of diethyl carbonate at ice bath temperature, then at room temperature for 2 days. To the dark solution is then added crushed ice and 5N hydrochloric acid to adjust the pH to 6-7. After dilution with diethyl ether, the layers are separated, the organic phase washed with a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. After removal of the solvents, the oily ethyl 3-(4-chloro-phenyl)-3-oxo-propionate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022801
Source datasetuspto-grants-1977_05
ORD IDord-de6f7cd047664e73a21e2219554aaa92
Source noteuspto-grants-1977_05