참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromoform | HCID 5558 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Dehydrolinalool | HCID 62842 | — |
| 촉매 | Benzyl triethylammonium chloride | HCID 66133 | — |
| 생성물 | 5-(2'2'-Dibromo-3'3'-dimethylcyclopropyl)-3-methyl-1-pentyn-3-ol | HCID 53803475 | 84.5% |
반응 단계
Dehydrolinalool (60.8 g, 0.4 mol), bromoform (151.6 g, 0.6 mol) and 0.8 g of triethylbenzylammonium chloride are placed in a reaction flask and 64 g of a 50% sodium hydroxide solution are added during 30 minutes. The reaction is exothermic and the mixture is therefore cooled with ice. After stirring the mixture at room temperature for 21.5 hours the same amounts of bromoform and triethylbenzylammonium chloride are again added. The reaction becomes exothermic and is cooled with ice. The mixture is left to react at 0° for a further 4 hours, poured onto ice and extracted with methylene chloride. The organic phases are washed neutral, dried and evaporated. In this manner there are obtained 109.5 g (84%) of 5-(2'2'-dibromo-3'3'-dimethylcyclopropyl)-3-methyl-1-pentyn-3-ol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05113021 |
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| 출처 데이터셋 | uspto-grants-1992_05 |
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| ORD ID | ord-d0890348fa134590832f593206ada504 |
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| 출처 메모 | uspto-grants-1992_05 |
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