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Sodium Hydroxide → O-Benzylhydroxylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Benzyloxyamine hydrochloride | HCID 102312 | — |
| 反応物 | 3-Hydroxypicolinaldehyde | HCID 2737332 | — |
| 溶媒 | Water ethanol | HCID 19096565 | — |
| 生成物 | O-Benzylhydroxylamine | HCID 102313 | — |
反応手順
A solution of O-benzyl hydroxylamine was prepared by dissolving 2 g of sodium hydroxide (0.05 mol) and 8 g of O-benzyl hydroxylamine hydrochloride (0.05 mol) in 50 mL of 50% ethanol-water. To this solution was added 6.15 g of 2-formyl-3-hydroxypyridine (0.05 mol). The mixture was stirred for 3 h at room temperature. The precipitate was then filtered and air dried to yield 10.3 g (90.3%) of pure product; m.p. 64°-65° C. 1H NMR (CDCl3) d: 9.72 (s, 1H, OH); 8.37 (s, 1H, CH=N); 8.13 (d of d, J=2H, J=4 Hz, 1H); 7.33 (m, 7H) 5.17 (s, 2H, CH2). Anal. Calcd. for C13H12N2O2 : C, 68.41; H, 5.30; N, 12.27. Found: C, 68.34; H, 5.32; N, 12.21.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05714615 |
| 出典データセット | uspto-grants-1998_02 |
| ORD ID | ord-276985d87d104f0e9e0e765265f526e0 |
| 出典メモ | uspto-grants-1998_02 |