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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26227Generated: October 25, 2026

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

https://huagongshe.com/reaction/26227

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 numberUS04148918
Source datasetuspto-grants-1979_04
ORD IDord-7baf14ecd86f45f5a549cee5a5e5b9b4
Source noteuspto-grants-1979_04