関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isobutylene oxide | HCID 11208 | — |
| 反応物 | Cyclohexanemethanol, alpha,3,3-trimethyl- | HCID 91338 | — |
| 反応物 | Ethyl aluminium dichloride | HCID 16686341 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | 2-[1-(3,3-Dimethyl-cyclohexyl)-ethoxy]-2-methyl-propan-1-ol | HCID 12022012 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07390779B2 |
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| 出典データセット | uspto-grants-2008_06 |
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| ORD ID | ord-c2a06d032eff4e9d975790186acbc953 |
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| 出典メモ | uspto-grants-2008_06 |
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