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HRID 1077150作成日:2026年10月25日

p-Toluenesulfonic acid → HCID 27234258、化合物

https://huagongshe.com/reaction/1077150

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物6-m-Acetoxyphenyl-1-diethylaminohexan-3-oneHCID 21485420—
反応物6-m-Acetoxyphenylhex-1-en-3-oneHCID 21485580—
反応物2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dioneHCID 21485772—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
生成物HCID 27234258HCID 27234258—

反応手順

Reflux 2-(6-m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione (0.8 g, the product of Michael condensation of 2-methylcyclopentanedione and a mixture of 6-m-acetoxyphenyl-1-diethylaminohexan-3-one and 6-m-acetoxyphenylhex-1-en-3-one, and containing some of the corresponding free phenolic compound) in benzene (25 cc) with toluene-p-sulfonic acid (0.3 g) for 50 minutes. On cooling add ether (50 cc) and wash the mixture in turn with water, saturated aqueous potassium bicarbonate, and brine; dry over anhydrous magnesium sulfate. The residue after removal of solvent is a purple gum (0.6 g), part of which can be induced to crystallize. Dissolve a portion (0.45 g) of this gum in benzene and adsorb on an activated Fuller's earth (40 g); elute with benzene to obtain 13β-methyl-3-hydroxygona-1,3,5(10),8,14-pentaen-17-one, which one recrystallizes from diisopropyl ether, m.p. 225°-226°; ultraviolet absorption peak at 312.5 mμ (ε23,000); infrared absorption peaks at 2.99 μ, 5.81 μ, and 8.00μ.

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-ff41c2cd4a0240ac8b97c3e893e2ffde
出典メモuspto-grants-1976_05