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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419948Generated: October 29, 2026

Sodium Dithionite → 2-[(6-Amino-2-chloro-3-fluorophenyl)amino]ethanol

https://huagongshe.com/reaction/419948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant2-((2-Chloro-3-fluoro-6-nitrophenyl)amino)ethan-1-olHCID 58298444—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[(6-Amino-2-chloro-3-fluorophenyl)amino]ethanolHCID 58298474—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-[(2-Chloro-3-fluoro-6-nitrophenyl)amino]ethanol (5.52 g, 22.7 mmol) is dissolved in MeOH (40.0 mL). A premixed solution of Na2S2O4 (13.8 g, 79.5 mmol) in water (40.0 mL) is added to the first solution. The resulting solution is stirred for 5 minutes at 60° C. followed by 2 hours at room temperature. The solvents are evaporated, and the resulting residue is suspended in a saturated solution of NaHCO3 (40.0 mL). The aqueous phase is extracted 4 times with EtOAc (4×40.0 mL). The combined organic phases are dried with MgSO4, filtered and concentrated. The product is sufficiently pure by 1H NMR (2.07 g, 45%). 1H NMR (400 MHz, DMSO-D6) δ ppm 2.99 (m, 2H) 3.32 (s, 1H) 3.48 (t, J=5.57 Hz, 2H) 4.09 (s, 1H) 4.73-4.95 (m, 2H) 6.55 (dd, J=8.79, 5.66 Hz, 1H) 6.71 (t, J=8.89 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093402B2
Source datasetuspto-grants-2012_01
ORD IDord-722c575360d94596b9ce2ff8ac6f2705
Source noteuspto-grants-2012_01