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Phosphorus trichloride → N-(1-Chloro-2,2,2-trifluoro-ethyl)-4-chlorobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphorus trichloride | HCID 24387 | — |
| 反応物 | 4-chloro-N-(2,2,2-trifluoro-1-hydroxyethyl)benzamide | HCID 11322758 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 溶媒 | Phosphorus oxychloride | HCID 24813 | — |
| 生成物 | N-(1-Chloro-2,2,2-trifluoro-ethyl)-4-chlorobenzamide | HCID 15906515 | 89.3% |
反応手順
A mixture of N-(1-hydroxy-2,2,2-trifluoroethyl)-4-chlorobenzamide (2.53 g, 0.01 mol) in phosphorus oxychloride (2 mL) is treated with phosphorus trichloride (1.57 g, 0.012 mol), heated to and held at 80° C. for 30 minutes, and concentrated in vacuo to obtain a residue. The residue is dissolved in hot heptane, decanted from the waxy phosphorus products, and crystallized to give the title product as a white crystalline solid (2.43 g, 89.3% yield): mp 119.0-121.0° C.; IR (Nujol) 3266, 1668 cm−1; 1H NMR (CDCl3) δ7.76 and 7.46 (AB with fine splitting, ArH), 6.86 (d, J=8.5 Hz, NH, moves to 10.24 in DMSO-d6), 6.55(m, CH); 19F NMR δ−77.7(d, J=5 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06596902B2 |
| 出典データセット | uspto-grants-2003_07 |
| ORD ID | ord-3f3bff3ff6974fe7bb1c51be54c797b4 |
| 出典メモ | uspto-grants-2003_07 |