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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834529Generated: October 25, 2026

Sulfuric Acid → Ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate

https://huagongshe.com/reaction/1834529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl AcetoacetateHCID 8868—
Reactanto-Tolyl-acetyl chlorideHCID 2760632—
ReactantMagnesiumHCID 5462224—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoateHCID 21325237—

Reaction Steps

This material was prepared according to the procedure of M. Viscontini and N. Merckling, Helvetica Chimica Acta, 35, 2280 (1952). To 2.65 parts of magnesium turnings was added 15 parts absolute ethanol at room temperature and 0.5 parts of carbon tetrachloride. As soon as the initial reaction subsides 100 parts of dry ether was added. The mixture was stirred without cooling until the reaction ceased, then 19.6 parts of ethyl 3-oxobutanoate in 20 parts of dry ether was added with ice cooling and good stirring. After the resulting precipitate dissolved, the solution was cooled in an ice-salt bath and 16 parts of 2-methylphenylacetyl chloride was slowly added. The mixture was allowed to stand overnight at room temperature and then combined with ice and sulfuric acid. The ether layer was separated, washed with water, dried over sodium sulfate and stripped to give ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate as a crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04070481
Source datasetuspto-grants-1978_01
ORD IDord-681e18fde8fb4c1eb1e47a54419fc093
Source noteuspto-grants-1978_01