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HRID 26227作成日:2026年10月26日

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

https://huagongshe.com/reaction/26227

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Ethyl AcetoacetateHCID 8868—
反応物o-Tolyl-acetyl chlorideHCID 2760632—
反応物MagnesiumHCID 5462224—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒Carbon TetrachlorideHCID 5943—
生成物Ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoateHCID 21325237—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04148918
出典データセットuspto-grants-1979_04
ORD IDord-7baf14ecd86f45f5a549cee5a5e5b9b4
出典メモuspto-grants-1979_04