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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905143생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/905143

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물2-Ethylhexanoyl chlorideHCID 79103—
반응물2-(2',5'-Dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 12876602—
촉매Dicyclohexano-18-crown-6HCID 85955—
용매BenzeneHCID 241—
용매Diethyl EtherHCID 3283—
생성물3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenoneHCID 2020651092.3%

반응 단계

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-ethylhexanoyl chloride was added, and the reaction mixture refluxed for 12 hrs. The reaction mixture was cooled to room temperature, taken up in 150 ml ether and 50 ml of water, washed three times with 0.25 N, NaOH, two times with water, two times with 6 N 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04422870
출처 데이터셋uspto-grants-1983_12
ORD IDord-d9aa4d897b7a423a83ed962dfc0becdd
출처 메모uspto-grants-1983_12