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Acetonitrile → N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium p-Toluene-sulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Methyl p-toluenesulfonate | HCID 6645 | — |
| 反応物 | N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N-methylamine | HCID 19962809 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium p-Toluene-sulfonate | HCID 19962811 | — |
反応手順
To a 250 ml round-bottomed flask fitted with a reflux condenser, magnetic stirrer, and argon inlet are added N,N-bis[2((phenoxycarbonyl)oxy)ethyl]-N-methylamine (25.00 g, 69.6 mmol), acetonitrile (100 ml), and methyl p-toluenesulfonate (12.95 g, 69.6 mmol). After addition is complete, the mixture is heated to reflux for 2 h. The cooled mixture is treated with ether (500 ml). The product precipitates from the mixture and dried to give 5 as a white powder, 31.14 g (81%): mp 117°-118° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05616546 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-e659b523b6ff4b2e9810a224ef5e9207 |
| 出典メモ | uspto-grants-1997_04 |