HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium Methylsulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N-methylamine | HCID 19962809 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium Methylsulfate | HCID 19962810 | — |
Reaction Steps
To a 1000 ml three-necked round-bottomed flask fitted with a reflux condenser, magnetic stiffer, 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 10 as a white powder, 126.26 g (93%): mp 85°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599781 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-14eb93c482f042c88fdbed7ddcc8ffa6 |
| Source note | uspto-grants-1997_02 |