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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833838Generated: October 26, 2026

Ethyl 5-cyano-4-oxo-5-(2-methylphenyl)pentanoate → 5-(2-Methylphenyl)-4-oxopentanoic acid

https://huagongshe.com/reaction/1833838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-cyano-4-oxo-5-(2-methylphenyl)pentanoateHCID 21387700—
SolventHydrogen BromideHCID 260—
Product5-(2-Methylphenyl)-4-oxopentanoic acidHCID 21387624—

Reaction Steps

Undistilled ethyl 5-cyano-4-oxo-5-(2-methylphenyl)pentanoate (prepared by the procedure described above; 773 g.) was heated under reflux with hydrobromic acid (48-50%; 1550 ml.) for 3 hours. On cooling, the reaction mixture separated into two layers. The lower, aqueous phase was separated and extracted with chloroform (3 × 500 ml.). The chloroform extract was added to the upper, organic layer of the reaction mixture. The chloroform solution (about 2 liters) thus obtained was washed with water (3 × 200 ml.) and evaporated to give 5-(2-methylphenyl)-4-oxopentanoic acid (535 g.) in the form of a dark coloured oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067723
Source datasetuspto-grants-1978_01
ORD IDord-6168301f8bbb46efa32d54cc5c9f6f71
Source noteuspto-grants-1978_01