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HRID 1077141作成日:2026年10月27日

Methanol → 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione

https://huagongshe.com/reaction/1077141

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物2-Methyl-1,3-cyclopentanedioneHCID 13005—
反応物6-m-Acetoxyphenyl-1-diethylaminohexan-3-oneHCID 21485420—
反応物6-m-Acetoxyphenylhex-1-en-3-oneHCID 21485580—
溶媒ChloroformHCID 6212—
溶媒Potassium HydroxideHCID 14797—
生成物2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dioneHCID 21485772—

反応手順

Reflux a mixture of 6-(m-acetoxyphenyl)-1-diethylaminohexan-3-one and 6-(m-acetoxyphenyl)hex-1-en-3-one (1 g), with 2-methylcyclopentane-1,3-dione (1.5 g) in 0.12% methanolic potassium hydroxide (6 cc) for 18 hours. Remove methanol (2 cc) under reduced pressure and add chloroform (60 cc). Wash the solution in turn with dilute sulfuric acid (25 cc), saturated potassium bicarbonate solution, and brine; dry and evaporate the solvent. The product (0.8 g) is the adduct 2-(6-m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione in admixture with some of the corresponding free phenol; infrared absorption: 2.86 to 3.08 (broad low-intensity band), 5.71, 5.81, 5.85, and 8.26 μ.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03959322
出典データセットuspto-grants-1976_05
ORD IDord-8782780bea62495b8605cb452e75635c
出典メモuspto-grants-1976_05