関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzylamine | HCID 7504 | — |
| 反応物 | Diethenyl(propan-2-yl)phosphane oxide | HCID 86658246 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-Benzyl-4-(propan-2-yl)-1,4-azaphosphinane 4-oxide | HCID 67432951 | 63% |
反応手順
A 20 L four-necked round bottom flask fitted with an overhead stirrer and reflux condenser, flame dried and cooled in a stream of nitrogen, was charged with the product of Step 1 (250 g, 1734 mmol), THE (2500 mL), water (2500 mL) and benzyl amine (297.3 g, 2774 mmol). The reaction mixture was heated at 85° C. for 16 h. After completion, THF was removed under reduced pressure. The aqueous layer was extracted with ether to remove the excess of benzyl amine and later with dichloromethane (2×2500 mL). The combined dichloromethane layers were washed with brine (2×1000 mL), dried over sodium sulfate and concentrated to give 1-benzyl-4-(propan-2-yl)-1,4-azaphosphinane 4-oxide (273 g, 63%) as brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08759366B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-6e6a6f8066e240b98b23069bdd4bbc05 |
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| 出典メモ | uspto-grants-2014_06 |
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