참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | N-(Tetrahydrofuran-3-yl)propionamide | HCID 21709920 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Propyl-N-(tetrahydrofuran-3-yl)amine | HCID 21709909 | — |
반응 단계
A suspension of 21.7 g (0.57 mol) of lithium aluminum hydride in 500 ml of THF was admixed dropwise with a solution of 81 g (0.57 mol) of N-(tetrahydrofuran-3-yl)propionamide, and the solution was heated at reflux for 2 h. Excess lithium aluminum hydride was hydrolyzed by dropwise addition of 16 ml of water, 50 ml of 10% strength aqueous sodium hydroxide solution and another 45 ml of water. The white suspension was heated at reflux for one hour, causing the insoluble components to aggregate to a coarse white precipitate. The mixture was filtered off from the precipitate, the precipitate was thoroughly rinsed with ether and the combined filtrates were distilled. B.p. 64° C. (12 mm), yield 41 g. 1H NMR (270 MHz, in CDCl3): δ=0.92 (t, 3H), 1.15 (s, 1H), 1.50 (sext., 2H), 1.70 (m, 1H), 2.10 (m, 1H), 2.55 (m, 2H), 3.38 (m, 1H), 3.56 (dd, 1H), 3.70-3.96 (m, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06277790B1 |
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| 출처 데이터셋 | uspto-grants-2001_08 |
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| ORD ID | ord-b88dadd5ce9e4356872d5cee917505c2 |
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| 출처 메모 | uspto-grants-2001_08 |
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