HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397299Generated: October 30, 2026
Sodium Dithionite → 3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline
https://huagongshe.com/reaction/1397299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 3-(3-Nitrophenyl)-5-(trifluoromethyl)-1,2,4-oxadiazole | HCID 550571 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline | HCID 20297549 | 57.2% |
Reaction Steps
Sodium dithionite (1.61 g, 9.2 mmol) and a catalytic amount of tetra-n-butylammonium bromide (20 mg) were added to a solution of 3-(3-nitrophenyl)-5-(trifluoromethyl)-1,2,4-oxadiazole (1.6 g, 6.1 mmol) in THF—H2O (30 mL, 1:1 v/v), and the reaction mixture was stirred at room temperature for 2 h and monitored by TLC (petroleum ether/EtOAc 1:1). Solvent was removed under reduced pressure and the product was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel 60-120 mesh, eluent 30-35% EtOAc in petroleum ether) to afford 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline (0.8 g, yield 57%). 1H NMR (300 MHz, CDCl3) δ 7.52-7.49 (dt, J=7.7 Hz, 1.2 Hz, 1H), 7.42 (m, 1H), 7.30 (t, J=8.0 Hz, 1H), 6.89-6.86 (ddd, J=7.9 Hz, 2.4 Hz, 0.9 Hz, 1H), 3.87 (br s, 2H). MS (ESI) m/z: Calculated for C9H6F3N3O: 229.05. found: 230.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08901156B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-d8d5fe73c02f4b54a502449235a1f286 |
|---|
| Source note | uspto-grants-2014_12 |
|---|