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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244938Generated: October 26, 2026

Pyridine → Ethyl 4,4-dimethyl-3-oxo-5-phenylpentanoate

https://huagongshe.com/reaction/244938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetoacetateHCID 8868—
ReactantMagnesium ChlorideHCID 5360315—
Reactant2,2-Dimethyl-3-phenylpropanoyl chlorideHCID 13307229—
SolventDichloromethaneHCID 6344—
ProductEthyl 4,4-dimethyl-3-oxo-5-phenylpentanoateHCID 8669746018%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 3-oxobutanoate (1.09 g, 8.3 mmol) in methylene chloride (16 mL) was mixed with anhydrous magnesium chloride (158 mg, 1.66 mmol), and the reaction solution was cooled to 0° C., mixed with pyridine (1.34 mL, 16.6 mmol), stirred for 30 minutes, then mixed with 2,2-dimethyl-3-phenylpropanoyl chloride (1.64 g, 8.3 mmol) and stirred for another 30 minutes at the same temperature. The reaction solution was warmed to room temperature and stirred for 20 hours. The methylene chloride was distilled off under reduced pressure, and the residue was with ethanol (2 mL) and at room temperature for 2 days and with toluene (2 mL) at 60° C. for 5 hours. After completion of the reaction, the reaction solution was washed with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate (50 mL×2). The solvent was removed from the resulting organic layer under reduced pressure, and the resulting brown oil was purified by intermediate pressure silica gel column chromatography (silica gel12 g, ethyl acetate:hexane=1:19 to 1:9) to give 370 mg of the desired product as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658686B2
Source datasetuspto-grants-2014_02
ORD IDord-f310f4dcb6274a00b1d15af426616c40
Source noteuspto-grants-2014_02