참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Piperidone | HCID 12665 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(Tetrahydro-2-oxo-3-furyl)-2-piperidinone | HCID 23342871 | 107% |
반응 단계
1.25 g (0.05 mol) of sodium hydride (2.5 g of a 50% commercial suspension in paraffin, previously washed twice with benzene) are suspended in 50 ml of anhydrous N,N-dimethylformamide. A solution of 4.95 g (0.05 mol) of 2-piperidinone in 20 ml of N,N-dimethylformamide is added dropwise to the suspension. The mixture is then heated to 60° C. until no more gas is evolved, whereafter it is cooled. A solution of 8.25 g (0.05 mol) of 3-bromodihydro-2(3H)-furanone in 20 ml of anhydrous N,N-dimethylformamide is added dropwise while keeping the temperature at 5° to 10° C. The mixture is then stirred at 60° C. for 5 hours. N,N-Dimethylformamide is evaporated off under reduced pressure. The residue is taken up in chloroform and the insoluble matter filtered off on Norit. The filtrate is again evaporated and 9.8 g of a heavy syrup are obtained. Mass spectrum: M+. at 183 m/e.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04221789 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-d71a5e4b990c4897a490adf4f3bc69d3 |
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| 출처 메모 | uspto-grants-1980_09 |
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