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HRID 371962作成日:2026年10月27日

Water → 1-Ethynylcyclohexene

https://huagongshe.com/reaction/371962

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物1-EthynylcyclohexeneHCID 79128—
反応物2,3,6-Trimethylcyclohexan-1-oneHCID 142583—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物1-EthynylcyclohexeneHCID 79128—
生成物1-(2,3,6-Trimethyl-1-hydroxy-cyclohexyl)-2-(cyclohex-1-en-1-yl)-acetyleneHCID 20352461—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04088681
出典データセットuspto-grants-1978_05
ORD IDord-c49b3e6afff64eb6bb4958e2c9f6e8a1
出典メモuspto-grants-1978_05