HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(2-hydroxyethyl)-N-methylmesitylenesulphonamide mesitylenesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2-hydroxyethyl)-N-methylmesitylenesulphonamide mesitylenesulphonate | HCID 23346524 | 1,622.9% |
Reaction Steps
66 g (0.3 mole) mesitylenesulphonyl chloride in 37.5 ml pyridine were added dropwise at -5° C. to 11.2 g (0.015 mole) 2-methylaminoethanol. The reaction mixture was kept in a cooler (4° C.) overnight and then poured on ice. 20 ml acetic acid were added and the product was washed with water, taken up in diethyl ether, washed with water and dried with Na2SO4. The solvent was removed in vacuum, giving 55.7 g pale yellow crystals of the title compound, m.p. 94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04218476 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-435aab59895f4f4e9f160e7a43157c0b |
| Source note | uspto-grants-1980_08 |