참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Isopropylphosphonic dichloride | HCID 2793751 | — |
| 반응물 | HCID 178418507 | HCID 178418507 | — |
| 생성물 | Diethenyl(propan-2-yl)phosphane oxide | HCID 86658246 | 80% |
반응 단계
A 20 L four-necked round bottom flask fitted with an overhead stirrer and dropping funnel, flame dried and cooled in a stream of nitrogen, was charged with isopropyl phosphonic dichloride (350.0 g, 2173 mmol) in THF (5000 mL). The mixture was cool to −78° C. and vinyl magnesium bromide (5217 mL, 5217 mmol, 1M in THF) was added dropwise over 4 h. The reaction mixture was stirred at −78° C. for additional 30 minutes. After completion, the reaction mixture was poured into cold saturated aqueous NH4Cl (3.5 L) and extracted with dichloromethane (4×1000 L). The organic layers were combined, washed with brine (2×15000 mL), dried over sodium sulfate and concentrated in vacuo to give diethenyl(propan-2-yl)phosphane oxide (250 g, 80%) as light-brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08551984B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-18bbf6a03b5e47e6affc00366dce04c8 |
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| 출처 메모 | uspto-grants-2013_10 |
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