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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161651Generated: November 1, 2026

Hydrochloric Acid → Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester

https://huagongshe.com/reaction/1161651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4'-MethoxyacetophenoneHCID 7476—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductBenzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 7615090.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-methoxyacetophenone (100 g, 0.66 mol) in dry dimethylformamide (400 mL), 60% sodium hydride (34.3 g, 0.85 mol) was added slowly at 10° C. under a nitrogen atmosphere. This mixture was stirred at 25° C. for 30 minutes and again cooled to 10° C. This was added to solution of diethyl carbonate (94.5 g, 0.80 mol) and dissolved in minimum quantity of dry dimethylformamide at the same temperature. The mixture was then stirred at 25° C. for 5 to 6 hours and poured into ice cold water (100 mL) with vigorous stirring. The mixture was then acidified (pH˜6-7) using cold 2 N hydrochloric acid and extracted with ethyl acetate. The organic layers were collected, combined, washed with water, dried over anhydrous sodium sulphate, filtered and concentrated under vacuum to afford the desired compound as yellow oil (133 g). Yield: 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820654B2
Source datasetuspto-grants-2010_10
ORD IDord-dcd3fdf5895349e7ac3c9f7a519ed5c6
Source noteuspto-grants-2010_10