HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,3,5-Trifluoro-6-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,2,3,5-Tetrafluoro-4-nitrobenzene | HCID 67566 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,5-Trifluoro-6-nitroaniline | HCID 223085 | 51% |
Reaction Steps
A solution comprising 2,3,4,6-tetrafluoronitrobenzene (0.6 g, 3.1 mmol) and ammonia in dioxane (Aldrich, 0.5M, 7.5 mmol) was stirred at room temperature for 3 hours to give a fine white precipitate. The mixture was diluted with an equal volume of water to dissolve the white precipitate and give yellow crystals. The crystals were isolated were collected and dried to provide 2,3,5-trifluoro-6-nitroaniline (307 mg, 51%) as yellow needles; m.p. 66° C.; 1H NMR (CDCl3) δ 6.4 (1H, m), δ 6.0 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562854B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-63bd390fc9ae4e0e94c0a4d53118d5a4 |
| Source note | uspto-grants-2003_05 |