HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 6-(Trifluoromethyl)quinolin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Chloro-6-(trifluoromethyl)quinoline | HCID 10911411 | — |
| Product | 6-(Trifluoromethyl)quinolin-2-amine | HCID 11218095 | 38% |
Reaction Steps
A solution of 2-chloro-6-(trifluoromethyl)quinoline (1 g, 4.3 mmol) in ammonium hydroxide (50 ml) was stirred overnight at 130° C. The resulting mixture was then concentrated under vacuum to give a residue, which was purified by silica gel column chromatography using 1%˜2% methanol in dichloromethane to afford 6-(trifluoromethyl)quinolin-2-amine as an off-white solid (350 mg, 38%). (ES, m/z): [M+H]+ 212; 1H NMR (300 MHz, CDCl3): δ 7.97-7.86 (m, 2H), 7.71 (s, 2H), 6.85 (d, J=9.0 Hz, 1H), 5.26 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249102B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-81e987ee77d34397b89df591172a69b4 |
| Source note | uspto-grants-2016_02 |