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HRID 2071225作成日:2026年10月27日

Methyl iodide → 3-Methyl-5-(2,6,6-trimethyl-2-cyclohexenyl)-4-penten-2-ol

https://huagongshe.com/reaction/2071225

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物3-Butenal, 2-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-HCID 93952—
反応物MagnesiumHCID 5462224—
反応物HCID 178418373HCID 178418373—
溶媒Diethyl EtherHCID 3283—
生成物3-Methyl-5-(2,6,6-trimethyl-2-cyclohexenyl)-4-penten-2-olHCID 5387838977.8%

反応条件

温度30 °C

反応手順

A solution of methylmagnesium iodide, prepared from 11 g of magnesium shavings and 76 g of methyl iodide, in 700 ml of absolute ether is added dropwise at -10° C. under nitrogen to a solution of 62 g of 2-methyl-4-(2,6,6-trimethyl-2-cyclohexenyl)-3-butenal in 700 ml of ether. The mixture is stirred for 4 hours at 30° C. and then poured on to an excess of ice-cold ammonium chloride solution. The mixture is extracted with ether in the usual manner, the extract is washed neutral with water and dried over anhydrous sodium sulphate to give, after removal of the solvent, 66 g of a yellow, slightly viscous oil which, after distillation in vacuo, yields 52 g of 3-methyl-5-(2,6,6-trimethyl-2-cyclohexenyl)-4-penten-2-ol; b.p.0.008 = 90°; nD20 = 1.4890. This alcohol has a very fine, tenacious sandalwood odour.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04046716
出典データセットuspto-grants-1977_09
ORD IDord-d74cf7cee1f44a459642b0b7cd91511f
出典メモuspto-grants-1977_09