戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 346818作成日:2026年10月26日

Water → 4-(2,4-Dihydroxyphenyl)cyclohexanone

https://huagongshe.com/reaction/346818

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物4-(1,4-Dioxaspiro[4.5]dec-8-yl)-1,3-benzenediolHCID 9921257—
溶媒AcetoneHCID 180—
生成物4-(2,4-Dihydroxyphenyl)cyclohexanoneHCID 9942489100%

反応手順

A flask equipped with magnetic stirrer was charged with 4-(1,4-dioxaspiro[4.5]dec-8-yl)-1,3-benzenediol (11.3 g, 45.2 mmol), acetone (250 ml) and water (50 ml). To the stirred solution was added pyridinium p-toluenesulfonate (1.14 g, e.52 mmol) in one portion and the reaction mixture as then heated under reflux for 8 hr. After allowing the reaction mixture to cool to room temperature, most of the acetone was removed in vacuo and the remaining mixture was partitioned between ethyl acetate (200 ml) and water (50 ml). The aqueous layer extracted with ethyl acetate (3 ×50 ml) and the combined organic layers were washed with brine (30 ml), dried (MgSO4), filtered and concentrated under reduced pressure to afford an off-white powder. After washing the powder with dichloromethane (100 ml) and removal of excess solvent under reduced pressure, the title compound (9.30 g, 100%) was obtained as an off-white powder. M/z (ES+) 207 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173052B2
出典データセットuspto-grants-2007_02
ORD IDord-99894fcc20fa47169198ab69853e9e3a
出典メモuspto-grants-2007_02