Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359992Generated: October 26, 2026

Ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate → 4-(2-(4-Methoxyphenyl)acetyl)-3-methylbenzonitrile

https://huagongshe.com/reaction/2359992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoateHCID 67174488—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product4-(2-(4-Methoxyphenyl)acetyl)-3-methylbenzonitrileHCID 6717417260.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a mixture of ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate (9F) (40 g, 0.1186 mol) in dimethyl sulfoxide (75 mL) was added catalytic amount of brine (2.5 mL), and the reaction mixture was heated at 150° C. for 2.5 h. When TLC showed the starting material was consumed, the reaction mixture was cooled down to room temperature, and partitioned between water (150 mL) and ethyl acetate (150 mL). The aqueous layer was extracted with ethyl acetate (100 mL×2). The combined organic layer was washed with brine (200 mL), dried over anhydrous sodium sulfate (15 g), evaporated, and purified by chromatography on silica gel (petroleum ether/ethyl acetate=25:1) to give 4-(2-(4-methoxyphenyl)acetyl)-3-methylbenzonitrile (9G) (19 g, yield 60.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686015B2
Source datasetuspto-grants-2014_04
ORD IDord-581541f5c5834bacb9eb042a23d7c460
Source noteuspto-grants-2014_04