戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 132980作成日:2026年10月26日

Isobutylene oxide → 2-[1-(3,3-Dimethyl-cyclohexyl)-ethoxy]-2-methyl-propan-1-ol

https://huagongshe.com/reaction/132980

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutylene oxideHCID 11208—
反応物Cyclohexanemethanol, alpha,3,3-trimethyl-HCID 91338—
反応物Ethyl aluminium dichlorideHCID 16686341—
溶媒TolueneHCID 1140—
溶媒CyclohexaneHCID 8078—
生成物2-[1-(3,3-Dimethyl-cyclohexyl)-ethoxy]-2-methyl-propan-1-olHCID 1202201238%

反応手順

At 0° C. under an atmosphere of nitrogen, 178 ml (321 mmol) of a 1.8 M solution of ethyl aluminium dichloride in toluene was slowly added to a stirred solution of 100 g (641 mmol) of 1-(3′,3′-dimethylcyclohexyl)ethanol and 55.4 g (769 mmol) of isobutylenoxide in 500 ml of cyclohexane. After complete addition, the cooling bath was removed, the reaction mixture was allowed to warm to room temperature, and stirring was continued at this temperature for 15 h. The reaction mixture was then poured into 1 L of brine, acidified with concentrated phosphoric acid, and thrice extracted with ether. The combined organic extracts were washed with brine and water, dried with sodium sulphate, and concentrated on a rotary evaporator. Distillation of the crude material (136 g) provided at 78-85° C./0.3 mbar 55.1 g (38%) of pure 2-[1′-(3″,3″-dimethylcyclohexyl)-ethoxy]-2-methylpropan-1-ol, while 60.4 g of starting material were recovered.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390779B2
出典データセットuspto-grants-2008_06
ORD IDord-c2a06d032eff4e9d975790186acbc953
出典メモuspto-grants-2008_06