関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-(4-Methylpiperazin-1-yl)aniline | HCID 286547 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 触媒 | Copper bromide (CuBr2) | HCID 24611 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-(2-Bromophenyl)-4-methylpiperazine | HCID 12069432 | — |
反応手順
A solution of 2-(4-methylpiperazin-1-yl)-aniline (23.77 grams, 0.124 mol) in 80 mL of 48% hydrobromic acid was cooled to 20° C. and treated with a solution of sodium nitrite (8.6 grams, 0.124 mol) in 35 mL of water while maintaining a temperature of 20-25° C. To this was added a solution of copper (II) bromide (3.5 grams, 0.024 mol) in 12 mL of 48% HBr. The mixture was heated to 85° C. for approximately 30 minutes, poured over crushed ice in a large beaker and neutralized with dilute aqueous sodium hydroxide. The crude product was extracted into diethyl ether and concentrated in vacuo to a black oil which was chromatographed on silica gel using triethylamine.methanol.methylene chloride (0.5:10:90) as the eluent. The product, 1-bromo-2-(4-methylpiperazin-1-yl)benzene, was obtained as a brown oil 20 grams Mass spectrum: 254 (M+), 256 1H-NMR (CDCl3, 300 MHz) δ 7.55 (1H, d), 7.30 (1H, t), 7.05 (1H, d), 6.9 (1H, t), 3.05 (4H, br s), 2.55 (4H, t), 2.35 (3H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06602874B2 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-66e6390c3d0f4e118c85e512c019fae9 |
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| 出典メモ | uspto-grants-2003_08 |
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