HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Methyl4-[4-(methylamino)-3-nitrophenoxy]pyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl5-[3-nitro-4-(2,2,2-trifluoroacetylamino)phenoxy]-pyridine-3-carboxylate | HCID 22040901 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Product | Methyl4-[4-(methylamino)-3-nitrophenoxy]pyridine-3-carboxylate | HCID 22040570 | — |
Reaction Steps
To the solution of the methyl5-[3-nitro-4-(2,2,2-trifluoroacetylamino)phenoxy]-pyridine-3-carboxylate (1 eq) in a mixture of toluene, acetonitrile and sodium hydroxide solution (50%) was added benzyltrimethylammonium chloride (1 eq) and dimethyl sulfate (1.2 eq). The biphasic mixture was stirred overnight at room temperature and evaporated. The mixture was taken up in ethyl acetate, washed with water, brine, dried and evaporated. The crude was purified by column chromatography to afford methyl-4-[4-(methylamino)-3-nitrophenoxy]pyridine-3-carboxylate. MS: MH+=303.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728010B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bf6dc933770b47d2a8ca9040f0f8e650 |
| Source note | uspto-grants-2010_06 |