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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267313Generated: October 28, 2026

Benzene → Mesityl oxide

https://huagongshe.com/reaction/267313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantMethyl acetoacetateHCID 7757—
ReactantMesityl oxideHCID 8858—
ReactantHeptaneHCID 8900—
CatalystZincchlorideHCID 3007855—
SolventWaterHCID 962—
ProductMesityl oxideHCID 8858—
ProductEthyl AcetoacetateHCID 8868—

Reaction Steps

A mixture of 2.6 kg. of methyl acetoacetate, 2.75 kg. of mesityl oxide, 400 g. of zinc chloride, 2 l. of heptane, and 2 l. of benzene was refluxed for 5 days. The water formed during the reaction was azeotropically distilled off and collected in a separator. A brown oily product remained in the flask. The oily product was then washed with water, sodium bicarbonate solution, and again with water. The oil which remained after washing was dried over calcium chloride and the heptane-benzene solvent removed under vacuum. The remaining oil was distilled under high vacuum over a packed column. From the distillation there was obtained first a forecut of unreacted ethyl acetoacetate and mesityl oxide, a second fraction of isophorone by product and finally crude 3,5,5-trimethyl-2-cyclohexen-1-on-4-carboxylic acid methyl ester with a boiling range of 95°-104° at 0.4-0.6 mm.Hg. This crude material was utilized for all experiments without further purification. Pure 3,5,5-trimethyl-2-cyclohexen-1-on-4-carboxylic acid methyl ester was obtained by chromatographic separation on silica gel G (finely divided powdered Silica containing trace amounts of calcium sulfate), using petroleum ether and ethyl ether in a volume ratio of 7 to 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03941841
Source datasetuspto-grants-1976_03
ORD IDord-79eb8c027b184d59b43820d9e72ba4c0
Source noteuspto-grants-1976_03