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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371962생성일: 2026년 10월 26일

Water → 1-Ethynylcyclohexene

https://huagongshe.com/reaction/371962

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1-EthynylcyclohexeneHCID 79128—
반응물2,3,6-Trimethylcyclohexan-1-oneHCID 142583—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-EthynylcyclohexeneHCID 79128—
생성물1-(2,3,6-Trimethyl-1-hydroxy-cyclohexyl)-2-(cyclohex-1-en-1-yl)-acetyleneHCID 20352461—

반응 단계

21.5 g of ethynylcyclohexene are added dropwise to a suspension of 6 g of 80% strength sodium hydride in 200 ml of tetrahydrofuran under reflux, and the reaction mixture is kept under reflux conditions until no further gas is evolved. 28 g of 2,3,6-trimethyl-cyclohexanone are then added dropwise at room temperature and the mixture is left overnight, whilst being stirred, in order to complete the reaction. Water is added to the reaction mixture, the reaction product is taken up in ether and the ether solution is washed with water, dried and concentrated. Fractional distillation gives 9 g of unconverted ethynylcyclohexene, 8 g of starting ketone, and 22 g of 1-(2,3,6-trimethyl-1-hydroxy-cyclohexyl)-2-(cyclohex-1-en-1-yl)-acetylene of boiling point 120° C/0.1 mm Hg and refractive index nD25 = 1.5143. This corresponds to a yield of 68% of theory, based on trimethylcyclohexanone converted. Fragrance note: faint, tart, herbaceous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04088681
출처 데이터셋uspto-grants-1978_05
ORD IDord-c49b3e6afff64eb6bb4958e2c9f6e8a1
출처 메모uspto-grants-1978_05