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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant3-(3-Nitrophenyl)-5-(trifluoromethyl)-1,2,4-oxadiazoleHCID 550571—
CatalystTetrabutylammonium BromideHCID 74236—
SolventOxolane--water (1/1)HCID 21881883—
Product3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)anilineHCID 2029754957.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-d8d5fe73c02f4b54a502449235a1f286
Source noteuspto-grants-2014_12