Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253250Generated: October 25, 2026

Hydrazine, dihydrochloride → HCID 178496107, compound

https://huagongshe.com/reaction/253250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, dihydrochlorideHCID 17548—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(3,4-Bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrileHCID 66890916—
SolventEthanolHCID 702—
ProductHCID 178496107HCID 17849610774%

Reaction Steps

To a solution of 2-(3,4-bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrile (0.57 g, 1.9 mmol) in ethanol (5 mL) was added hydrazine dihydrochloride (0.20 g, 2.2 mmol) The resulting mixture was heated at reflux for 1 hour. It was cooled, pour into a saturated sodium bicarbonate solution (10 mL), and the mixture was extracted with ethyl acetate (3×10 mL). The combined extract was washed with aqueous sodium bicarbonate solution, brine, dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (silica gel, 5% methanol-dichloromethane) to provide 4-(3,4-bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-methyl-1H-pyrazol-5-amine (0.46 g, 1.4 mmol, 74% yield). 1H NMR (400 MHz, CDCl3): 6.96-6.92 (m, 2H), 6.87-6.84 (d, d, 1H), 4.19-4.16 (m, 4H), 3.79-3.76 (m, 4H), 3.67 (s, 2H), 3.46 (s, 3H), 3.44 (s, 3H), 2.25 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-6c4ac2695bbe47ee837fa085a8e1b589
Source noteuspto-grants-2011_01