HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Phenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 2-(3-Pyridinyloxy)-5-(trifluoromethyl)aniline | HCID 26189415 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamate | HCID 59588873 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A yellow solution of 2-(pyridin-3-yloxy)-5-(trifluoromethyl)aniline (263 mg, 1.035 mmol) and pyridine (108 μL, 1.341 mmol) in dry THF (8 mL) was treated dropwise with phenyl chloroformate (156 μL, 1.242 mmol) during 5 min at 0° C. The resulting suspension yellow suspension was stirred at 0° C. for an additional 5 min and then allowed to warm up to room temperature and stirred for 3 h. The yellow suspension was filtered over cotton, washed with Et2O and diluted with EtOAc. The yellow solution was washed with sat. aqueous NaHCO3 (30 mL) and H2O (30 mL), dried and concentrated to dryness to give a yellow oil. Purification by column gave a tan solid. Yield: 300 mg (77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198279B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-d1c7a08ed469478ba74e61b4ef4b22f7 |
| Source note | uspto-grants-2012_06 |