HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylamine → [[4-[[4-Chloro-2-[[5-[4-(trifluoromethyl)phenyl]-2,3-dihydro-2-oxo-1,3,4-oxadiazol-3-yl]methyl]phenoxy]carbonyl]phenyl]-methyl] trimethylammonium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | 4-Chloro-2-[[5-[4-(trifluoromethyl)phenyl]-2,3-dihydro-2-oxo-1,3,4-oxadiazol-3-yl]methyl]phenyl 4-(chloromethyl)benzoate | HCID 21852100 | — |
| Solvent | Acetonitrile ethyl acetate | HCID 21930812 | — |
| Product | [[4-[[4-Chloro-2-[[5-[4-(trifluoromethyl)phenyl]-2,3-dihydro-2-oxo-1,3,4-oxadiazol-3-yl]methyl]phenoxy]carbonyl]phenyl]-methyl] trimethylammonium chloride | HCID 9808417 | 72% |
Reaction Steps
A solution of 4-chloro-2-[[5-[4-(trifluoromethyl)phenyl]-2,3-dihydro-2-oxo-1,3,4-oxadiazol-3-yl]methyl]phenyl 4-(chloromethyl)benzoate (0.3 g, 0.573 mmol) in acetonitrile/ethyl acetate (20 mL) was saturated with anhydrous trimethylamine. The reaction mixture was stirred at room temperature for two days. The precipitate was collected and purified by recrystallization from acetonitrile-ether to afford the title compound as a white solid (0.24 g, 72%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05948802 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-64dfe40c41c147cd8fefffcf9919c0a9 |
| Source note | uspto-grants-1999_09 |