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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835446Generated: October 31, 2026

Sodium Bicarbonate → 3-(Pyridazin-4-yl)phenylamine

https://huagongshe.com/reaction/1835446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3,6-Dichloro-4-(3-nitro-phenyl)pyridazineHCID 13634837—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-(Pyridazin-4-yl)phenylamineHCID 1363483988.3%

Reaction Steps

A suspension of 3,6dichloro4-(3-nitro-phenyl)pyridazine (0.19 g) and sodium hydrogen carbonate (147 mg) in tetrahydrofuran (2 ml) and ethanol (5 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 100 mg) under hydrogen atmosphere for 3 hours. The catalyst was filtered off, and the filtrate was evaporated. The residue was diluted with ethyl acetate and an aqueous solution of sodium hydrogen carbonate. The separated organic layer was washed with brine and dried over potassium carbonate. The organic layer was evaporated under reduced pressure to give 3-(pyridazin-4-yl)phenylamine (106 mg, 88.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770667B1
Source datasetuspto-grants-2004_08
ORD IDord-508a0c27b2fe4ff98a11ae341c533faa
Source noteuspto-grants-2004_08