HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → N,N-Bis[2-((phenoxycarbonyl)oxy)ethyl]-N,N-dimethylammonium p-Toluene-sulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| 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 p-Toluene-sulfonate | HCID 19962811 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05595967 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-f9458d1077c043beb177ab0ffce4a753 |
| Source note | uspto-grants-1997_01 |