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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465438Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-(4-acetonylphenyl)-2-chloropropionate

https://huagongshe.com/reaction/465438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-(Bromomethyl)phenyl)propan-2-oneHCID 19874489—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(4-acetonylphenyl)-2-chloropropionateHCID 19874575—

Reaction Steps

A solution of ethyl 2-chloroacetoacetate (8.25 g) in dry dimethylformamide was treated with sodium hydride (1.3 g and stirred at ambient temperature for 0.5 h. A solution of 4-(bromomethyl)phenylpropan-2-one, ethylene ketal (12.0 g) in dry dimethylformamide (20 ml) was then added and the mixture was heated at 70° C. for 4 h. The reaction mixture was cooled, poured into ice/water, acidified with 2N-hydrochloric acid, extracted with ethyl acetate (4×50 ml) and the combined organic extracts dried (magnesium sulphate), filtered and evaporated in vacuo. The residue was dissolved in ethanol and treated at 0°-5° C. with barium hydroxide hydrate (7.7 g). The mixture was stirred for 0.5 h, poured into ice/water, extracted with ethyl acetate (3×50 ml) and the combined organic extracts dried (magnesium sulphate), filtered and evaporated in vacuo to leave a red oil, which was purified by column chromatography on silica using diethyl ether: petroleum ether (60°-80°) (30:70) as eluent to give ethyl 3-(4-acetonylphenyl)-2-chloropropionate, ethylene ketal, (6.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153210
Source datasetuspto-grants-1992_10
ORD IDord-be8b5aa939354b438e2ad3827832cb73
Source noteuspto-grants-1992_10