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HRID 23601作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/23601

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PyridiniumHCID 4989215—
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 ptoluenesulfonate (1.14 g, 4.52 mmol) in one portion and the reaction mixture was 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 was 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US06852747B2
出典データセットuspto-grants-2005_02
ORD IDord-32c46541876143f2a74bd1c8b6397d98
出典メモuspto-grants-2005_02