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Triethylamine → methyl 4-[N-[2-(3-cyanophenoxy)ethyl)carbamoyl]benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-(2-Aminoethoxy)benzonitrile hydrobromide | HCID 17788773 | — |
| 反応物 | Monomethyl terephthalate chloride | HCID 22493623 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | methyl 4-[N-[2-(3-cyanophenoxy)ethyl)carbamoyl]benzoate | HCID 68830761 | — |
反応手順
1.50 g (6.2 mmol) of 3-(2-aminoethoxy)benzonitrile hydrobromide and 3 ml of triethylamine were stirred in 15 ml of dimethylformamide under cooling with ice. 1.23 g (6.2 mmol) of monomethyl terephthalate chloride was slowly added thereto, and they were stirred for 3 hours. The temperature was elevated to the room temperature, and the reaction liquid was diluted with 1 N hydrochloric acid. After the extraction with ethyl acetate, the organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and then with saturated aqueous NaCl solution, and then dried over anhydrous magnesium sulfate. The solvent was evaporated to obtain the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07396844B1 |
| 出典データセット | uspto-grants-2008_07 |
| ORD ID | ord-5ebf417277be4a51b4f7be0c7c0f2d75 |
| 出典メモ | uspto-grants-2008_07 |