関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Tetraethyl methylenediphosphonate | HCID 15455 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Hydride | HCID 166653 | — |
| 反応物 | N-butyl-2-chloroacetamide | HCID 219645 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-butyl-3,3-bis(diethoxyphosphinyl)propionamide | HCID 19689044 | 70% |
反応手順
Tetraethyl methylenebisphosphonate (1.44 g, 5.0 mmol) in THF (1 mL) was added to a slurry of 80% sodium hydride (150 mg, 5.0 mmol) in THF (4 mL) at 0° C. The reaction was warmed to room temperature and stirred until all of the hydride was consumed. A solution of N-butyl-2-chloroacetamide (0.75 g, 5.0 mmol) in THF (1 ml) and potassium iodide (100 mg) were then added. The reaction mixture was then heated at 50° C. for 18 hours, during which time sodium chloride precipitated. Additional sodium hydride (20 mg) was added, and the reaction mixture was heated an additional 4 hours. After cooling, the mixture was poured into 1N HCl (10 mL) and diethyl ether (50 mL) was added. The diethyl ether layer was further extracted with water (3×10 mL). The combined aqueous fractions were extracted with dichloromethane (4×25 mL). The combined extracts were dried (Na2SO4) and concentrated to give the title compound (1.40 g, 70%) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05728650 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-0d06fa7cb400433aac9523d5cb4e75c0 |
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| 出典メモ | uspto-grants-1998_03 |
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