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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26227Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/26227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl AcetoacetateHCID 8868—
Edukto-Tolyl-acetyl chlorideHCID 2760632—
EduktMagnesiumHCID 5462224—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktEthyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoateHCID 21325237—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04148918
Quelldatensatzuspto-grants-1979_04
ORD IDord-7baf14ecd86f45f5a549cee5a5e5b9b4
Quellennotizuspto-grants-1979_04