참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | 6-Methoxy-1-Indanone | HCID 334036 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 촉매 | zinc(II)iodide | HCID 9883512 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 1-(Aminomethyl)-2,3-dihydro-6-methoxy-1H-inden-1-ol | HCID 53638837 | — |
반응 단계
60 g of trimethylsilyl cyanide are added via syringe to a mixture of 75 g of 6-methoxy-1-indanon, 0.8 g of anhydrous zinc iodide and 150 milliliters of anhydrous toluene. The reaction mixture was heated to 60 degrees Centrigrade for 6 hours and then stirred for 16 hours without heating. To a cooled suspension of 44 g of lithium aluminium hydride in 1300 milliliters of anhydrous ether was added the solution of the unpurified cyanohydrin in ether at 0°-5° C. After the addition had been completed the reaction mixture was refluxed with stirring for 21/2 hours. After cooling destruction of the excess lithium aluminium hydride was completed by cautious dropwise addition of 45 milliliters of water followed by dropwise addition of 45 milliliters of 14% sodiumhydroxide solution and subsequent addition of 190 milliliters of water. Stirring was continued for 30 minutes. Filtration and extraction with dichloromethane gave a clear organic solution which was dried over anhydrous magnesium sulphate and evaporated, and the residue was crystallized from ether. Yield: 58 grams of product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04946863 |
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| 출처 데이터셋 | uspto-grants-1990_08 |
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| ORD ID | ord-8d6b80f21d9348f588746c8b6b347701 |
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| 출처 메모 | uspto-grants-1990_08 |
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