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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574091Generated: October 29, 2026

Sodium Dithionite → HCID 86669367, compound

https://huagongshe.com/reaction/574091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantHCID 86669360HCID 86669360—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 86669367HCID 8666936761.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of (3-allyloxy-5,6-difluoro-2-nitro-phenyl)-(4-iodo-phenyl)-amine (Intermediate 9, 1.1 g, 2.5 mmol) in ethanol (15 mL) was stirred at 70° C. to obtain a clear solution. To this hot solution, was added a freshly prepared solution of Na2S2O4 (1.3 g, 7.6 mmol) in water (3.1 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, and the organic phase was dried over anhydrous Na2SO4 and concentrated to yield 6-allyloxy-3,4-difluoro-N2-(4-iodo-phenyl)-benzene-1,2-diamine as a brown solid (620 mg). 1H-NMR (400 MHz, CDCl3): δ 4.54 (2H, d, J=4.8), 5.24 (1H, s), 5.32 (1H, d, J=10.8), 5.42 (1H, d, J=17.2), 6.06-6.02 (1H, m), 6.45 (2H, d, J=8.4), 6.57-6.62 (1H, m), 7.47 (2H, d, J=8.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034861B2
Source datasetuspto-grants-2015_05
ORD IDord-4747803678da4566988c0f7ebafa3667
Source noteuspto-grants-2015_05