関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Methyldiethanolamine | HCID 7767 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Phenyl chloroformate | HCID 15891 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N-methylamine | HCID 19962809 | — |
反応手順
To a 500 ml three-necked round-bottomed flask equipped with an internal thermometer, reflux condenser, mechanical stirrer, addition funnel, and argon inlet are added N-methyldiethanolamine (20.00 g, 0.168 mol), toluene (200 ml), and triethylamine (37.36 g, 0.369 mol). The minute is treated with a solution of phenylchloroformate (52.56 g, 0.336 mol dissolved in 50 ml of toluene so as to maintain the reaction temperature at 35°-45° C. After addition is complete, the mixture is heated at 45° C. for an additional 1.5 h. The cooled mixture is washed with saturated sodium bicarbonate solution (2×200 ml) and water (200 ml). The organic phase is dried over MgSO4, filtered, and concentrated first by rotary evaporation at 50° C. (water aspirator vacuum) and then at 80° C. (0.02 mmHg) in a Kugelrohr oven to give 3 as a light yellow oil, 55.65 g (92%) that crystallizes on standing.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05616546 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-2085c51b61b847ae9cb53b95d77445f8 |
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| 出典メモ | uspto-grants-1997_04 |
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