関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | P-Anisidine | HCID 7732 | — |
| 反応物 | Bromoacetyl bromide | HCID 61147 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-bromo-N-(4-methoxyphenyl)acetamide | HCID 532213 | — |
反応手順
The title compound was prepared via a modification of the literature procedure (Vloon, W. J.; Kruk, C.; Pandit, U. K.; Hofs, H. P.; McVie, J. G. J. Med Chem. 1987, 30, 20-4.). To a solution of 4-methoxyaniline (4.93 g, 40.0 mmol) in methylene chloride (200 mL) was added diisopropylethylamine (7.66 mL, 44.0 mmol). The resulting mixture was cooled to -20° C., and bromoacetyl bromide (3.82 mL, 44.0 mmol) was added slowly. The reaction mixture was warmed to room temperature over 20 minutes and stirred additional 30 minutes. The reaction mixture was diluted with water (100 mL), stirred for 30 minutes and the organic layer was separated. The organic layer was washed with water (2×100 mL), brine (100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (9.68 g) which was recrystallized from ethyl acetate to provide bromo-N-(4'-methoxyphenyl)acetamide as a whim crystal (6.31 g, 65%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05731438 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-a73c3e09e44447508491ea934b7c975c |
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| 出典メモ | uspto-grants-1998_03 |
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