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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574090Generated: October 31, 2026

Sodium Dithionite → HCID 86669366, compound

https://huagongshe.com/reaction/574090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantHCID 86669359HCID 86669359—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 86669366HCID 8666936699.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of (3-allyloxy-5,6-difluoro-2-nitro-phenyl)-(4-bromo-2-fluoro-phenyl)-amine (Intermediate 8, 0.7 g, 1.7 mmol) in ethanol (12 mL) was stirred at 70° C. to obtain a clear solution. To this hot solution, was added a freshly prepared solution of Na2S2O4 (0.9 g, 5.2 mmol) in water (1.9 mL) and stirred the reaction mixture at 90° C. for 1 h. The progress of reaction was monitored by TLC. After completion, the solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate, washed with water, dried over anhydrous Na2SO4 and concentrated to yield 6-allyloxy-N2-(4-bromo-2-fluoro-phenyl)-3,4-difluoro-benzene-1,2-diamine as a yellow solid (630 mg). 1H-NMR (400 MHz, CDCl3): δ 4.55 (2H, d, J=5.6), 5.32-5.36 (2H, m), 5.42 (1H, d), 6.02-6.08 (1H, m), 6.35 (1H, t, J=8.8), 6.60-6.65 (1H, m), 7.06 (1H, d, J=8.4), 7.23 (1H, dd, J=2.0, 10.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034861B2
Source datasetuspto-grants-2015_05
ORD IDord-f8a9e9c545a546b187328f1636ab5e4f
Source noteuspto-grants-2015_05