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Acetonitrile → N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium Methylsulfate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 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 Methylsulfate | HCID 19962810 | — |
反応手順
To a 1000 ml three-necked round-bottomed flask fitted with a reflux condenser, magnetic stirrer, internal thermometer, addition funnel, and argon inlet are added N,N-bis[2-((phenoxycarbonyl)oxy)ethyl]-N-methylamine (100.00 g, 0.278 mol), acetonitrile (270 ml), and dimethylsulfate (35.93 g, 0.278 mol) over 10 min. 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 after approximately 15 min to give 4 as a white powder, 126.26 g (93%): mp 85°-87° 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-02cacc73113c408c9974ae03a4320444 |
| 出典メモ | uspto-grants-1997_04 |