HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Difluoromethyl-5-(2-fluoro-6-nitro-phenyl)-5,6-dihydro-2H-[1,4]oxazin-3-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 5-Difluoromethyl-5-(2-fluoro-phenyl)-5,6-dihydro-2H-[1,4]oxazin-3-ylamine | HCID 66665906 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Difluoromethyl-5-(2-fluoro-6-nitro-phenyl)-5,6-dihydro-2H-[1,4]oxazin-3-ylamine | HCID 86716534 | 97.9% |
Reaction Steps
Potassium nitrate (60.3 g, 596 mmol) was added portionwise to 600 ml sulfuric acid (Temperature<20° C.). This solution was added dropwise to a solution of 5-difluoromethyl-5-(2-fluoro-phenyl)-5,6-dihydro-2H-[1,4]oxazin-3-ylamine (112 g, 459 mmol) in 600 ml sulfuric acid, while keeping the reaction temperature<22° C. with an ice bath. After stirring for 1 h, the mixture was poured onto 10 Kg ice. TBME (6 L) was added and the pH was adjusted to 12-14 by the addition of about 5 L 30% aqueous NaOH. The phases were separated and the aqueous phase was extracted twice with TBME. The combined organic layers were dried with sodium sulfate and evaporated to give 130 g of a yellow solid that was used further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846658B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7c9ad58649224f3dbd34ce78307b90d5 |
| Source note | uspto-grants-2014_09 |