化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → n-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| 反応物 | N-(4-Methoxyphenyl)-2-hydroxybenzamide | HCID 478806 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | n-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamide | HCID 18174417 | 61% |
反応手順
To a solution of N-(4-methoxyphenyl)-2-hydroxybenzamide (0.484 g, 2.00 mmol) in methylene chloride (35 mL) cooled to 0° C. was added 0.28 mL triethylamine (0.28 mL, 2.0 mmol), followed by the dropwise addition of a solution of 4-tert-butylbenzoyl chloride (0.393 mL, 2.00 mmol) in methylene chloride (15 mL). The reaction mixture was allowed to warm to room temperature over 16 h and washed with cold water. The organic layer was dried (magnesium sulfate), filtered, and concentrated in vacuo. Trituration with hexane provided 0.488 g (61%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06605626B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-933d062ec3704b6babb191877ecf3135 |
| 出典メモ | uspto-grants-2003_08 |