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HRID 1414958생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1414958

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2-Methyl-1,3-cyclopentanedioneHCID 13005—
반응물6-m-Acetoxyphenyl-1-diethylaminohexan-3-oneHCID 21485420—
반응물6-m-Acetoxyphenylhex-1-en-3-oneHCID 21485580—
용매ChloroformHCID 6212—
용매Potassium HydroxideHCID 14797—
생성물2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dioneHCID 21485772—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04002746
출처 데이터셋uspto-grants-1977_01
ORD IDord-bd5a066270e1404bb3a2ccbce35d50b6
출처 메모uspto-grants-1977_01