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Acetic Anhydride → N-(1-(4-bromophenyl)propan-2-yl)acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 4-Bromo-alpha-methylbenzeneethanamine | HCID 205668 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | N-(1-(4-bromophenyl)propan-2-yl)acetamide | HCID 45824256 | — |
反応手順
17.0 mL (179.7 mmol) acetic anhydride are added to a mixture of 24.2 g (113 mmol) 1-(4-bromophenyl)propane-2-amine and 20 mL AcOH and the reaction mixture is stirred at r.t. over night. The solvent is evaporated in vacuo, and the residue partitonated between TBME and a saturated aq. NaHCO3 solution. The layers are separated and the organic layer is washed with water, dried with Na2SO4, filtered and the solvent is removed in vacuo. The crude product is triturated with DIPE.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08623860B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-5ed5faccfa8741a89d4252efa52b52aa |
| 出典メモ | uspto-grants-2014_01 |