HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Bromo-5-fluoro-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59821153 | HCID 59821153 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-5-fluoro-2-nitroaniline | HCID 21911928 | 84% |
Reaction Steps
To N-(4-bromo-5-fluoro-2-nitrophenyl)-2,2,2-trifluoroacetamide (3.5 g, 10.5 mmol) was added CH3OH (30 mL) followed by 1.0 M K2CO3 (10.5 mL, 10.5 mmol), and the solution was stirred for 30 minutes (Charifson, P. S.; et al. J. Med. Chem. 2008, 51, 5243-5263). The solution was diluted with H2O and stirred for 1 hour. The resulting orange solid was collected by filtration and dried in a vacuum oven to give the title compound (2.1 g, 8.8 mmol, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394279B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-e5b21de656bb44189d05111cf1900ce8 |
| Source note | uspto-grants-2016_07 |