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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54311Generated: October 31, 2026

Benzene → 3,4,5,6-Tetrafluorobenzene-1,2-diamine

https://huagongshe.com/reaction/54311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
Reactant2,3,4,5-Tetrafluoro-6-nitroanilineHCID 2775760—
ReactantCalcium ChlorideHCID 5284359—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3,4,5,6-Tetrafluorobenzene-1,2-diamineHCID 2773957—

Reaction Steps

3,4,5,6-Tetrafluoro-1,2-diaminobenzene was prepared using an adaptation of the method of Tsuji et al., J. Org. Chem. 55:580 (1990). A suspension of Zn powder (1.95 g, 29.8 mmol), CaCl2 (195 mg) and H2O (2.3 mL) in 7 mL EtOH was heated m reflux with stirring under N2. To this was added slowly dropwise a solution of 2-nitro-3,4,5,6-tetrafluoroaniline (2 g, 12.8 mmol) in 5 mL EtOH. The reaction mixture was refluxed 5 h. TLC analysis (silica gel, 2:1 benzene:EtOAc) indicated complete disappearance of the starting material. The Zn was removed by vacuum filtration, and the Zn rinsed with EtOH (30 mL). The solvent was rotary evaporated and the residue was dissolved in 20 mL Et2O and the solution washed with 2×15 mL H2O and 15 mL sat'd NaCl. The organic layer was dried (MgSO4) and vacuum filtered. The solvent was rotary evaporated to yield 396.6 mg (92.5%) of a purple brown solid, mp 120°-125° C., that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622952
Source datasetuspto-grants-1997_04
ORD IDord-92f9d41425274def918f4085b9a6f301
Source noteuspto-grants-1997_04