참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3H-1,2-dihydro-1-pyrrolizinone | HCID 97347 | — |
| 반응물 | Methylenetriphenylphosphorane | HCID 137960 | — |
| 촉매 | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2,3-dihydro-1-methylene-1H-pyrrolizine | HCID 20270355 | — |
반응 단계
A solution of 2,3-dihydro-1-oxo-1H-pyrrolizine (16.1 g, 0.133 m); J. Org. Chem., 27 2468 (1962) ) in dried dimethylsulfoxide (60 ml) is added dropwise over ca. 10 minutes to a mixture of methylenetriphenylphosphorane (from methyl triphenylphosphonium bromide (57.2 g, 0.16 m), sodium hydride 60% dispersion (6.4 g, 0.16 m) and dimethylsulfoxide (256 ml) in the standard fashion (J. Org. Chem., 28 1128 (1963)) at ambient temperatures. After stirring for ca 2 hours, the mixture is heated in an oil-bath set at 70° C. for ca 30 minutes, and let cool. After stirring overnight at ambient temperatures, the mixture is poured into 1200 ml of ice-water, extracted 4×400 ml of ether, the ether layers washed 3×400 ml of water, dried and concentrated to a residue. The residue is extracted well with hexane, the filtered hexane extracts concentrated and distilled to yield 2,3-dihydro-1-methylene-1H-pyrrolizine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04536512 |
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| 출처 데이터셋 | uspto-grants-1985_08 |
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| ORD ID | ord-4158bf6627e24c25875e6801c3c29dee |
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| 출처 메모 | uspto-grants-1985_08 |
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