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HRID 542674作成日:2026年10月27日

Potassium Hydroxide → 3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone

https://huagongshe.com/reaction/542674

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物2-Ethylhexanoyl chlorideHCID 79103—
反応物2-(2',5'-Dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 12876602—
触媒Dicyclohexano-18-crown-6HCID 85955—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
生成物3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenoneHCID 2020651092.3%

反応手順

A suspension of 1.50 g (6.14 mmol) of 2-(2',5'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 15 ml of dry benzene was prepared and 0.49 g (7.37 mmol) of 85% powdered potassium hydroxide was added, followed by 1 drop of dicyclohexyl-18-crown-6-ether. After stirring for 30 minutes, 1.20 g (7.37 mmol) of 2-ethyl-hexanoyl chloride was added, and the reaction mixture refluxed for 12 hours. The reaction mixture was cooled to room temperature, taken up in 150 ml ether and 50 ml of water, washed three times with 0.25N NaOH, two times with water, two times with 6N HCl, and once more with water. The ether solution was dried and stripped to leave 2.10 g (92% yield) of 3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone as a clear, colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04659372
出典データセットuspto-grants-1987_04
ORD IDord-a7e0094617524557a994ca1e9ca6ffbf
出典メモuspto-grants-1987_04