HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → N-(1-methoxy-2,2,2-trifluoroethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2,2,2-Trifluoroacetaldehyde hydrate | HCID 2781366 | — |
| Reactant | 4-Methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide | HCID 18326229 | — |
| Product | N-(1-methoxy-2,2,2-trifluoroethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide | HCID 18326218 | — |
Reaction Steps
4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide was dissolved in benzene and mixed with 0.36 g (0.0026×1.2 mol) of trifluoroacetaldehyde hydrate, followed by treating the obtained solution under reflux for about 5 hours. The reaction solution was concentrated and then distributed in ethyl acetate-saturated sodium bicarbonate water, followed by washing with saturated brine. The organic phase of the obtained solution was dried with anhydrous sodium sulfate, concentrated and purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06339045B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-e645bd9b7e22498b9d4dcd93fda32a2c |
| Source note | uspto-grants-2002_01 |