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Triethylamine → N-[2-[2-Cyanophenoxy]phenyl]-4-hexyloxybenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Benzoyl chloride, 4-(hexyloxy)- | HCID 170235 | — |
| 反応物 | 2-(2-Aminophenoxy)benzonitrile | HCID 20084388 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | N-[2-[2-Cyanophenoxy]phenyl]-4-hexyloxybenzamide | HCID 20084541 | 77.3% |
反応手順
In 20 ml of ether was dissolved 2.0 g of 2-(2-aminophenoxy)benzonitrile followed by addition of 2.04 g of triethylamine. Then, with ice-cooling and stirring, a solution of 2.67 g of 4-hexyloxybenzoyl chloride in 5 ml of ether was added dropwise. The mixture was further stirred at the same temperature for 1 hour. The reaction mixture was then washed with diluted hydrochloric acid and aqueous sodium hydrogen carbonate solution in that order, dried and concentrated. The residue was purified by silica gel column chromatography using ethyl acetate-n-hexane as the eluent and the relevant fraction was crystallized from diisopropyl ether to give 3.05 g of the title compound as white crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05399703 |
| 出典データセット | uspto-grants-1995_03 |
| ORD ID | ord-5b022dcb1f1d4d9ba8c88d9364ccec6c |
| 出典メモ | uspto-grants-1995_03 |