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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28394Generated: October 26, 2026

Methylhydrazine → 4-(1-Methyl-6-oxo-1,6-dihydropyridazin-3-yl)benzoic acid

https://huagongshe.com/reaction/28394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
Reactant4-Acetylbenzoic AcidHCID 11470—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventAcetic AcidHCID 176—
Product4-(1-Methyl-6-oxo-1,6-dihydropyridazin-3-yl)benzoic acidHCID 67104487—

Reaction Conditions

Temperature40 °C

Reaction Steps

4-Acetylbenzoic acid (5.00 gram, 30.5 mmol) and 3.19 gram of glyoxalic acid monohydrate (34.7 mmol, 1.14 eq.) were stirred in 50 mL of acetic acid at 110° C. for 20 hours, and then cooled to 40° C. Solvent was removed with evaporator in vacuo. To the residue was added water (15 mL), and the mixture cooled with an ice bath. The resulting solution was titrated with ammonia solution until pH 9. Methyl hydrazine (3.00 mL 57.3 mmol, 1.88 eq.) was added, and the mixture was heated to reflux for 5 hours. The solution was concentrated in vacuo. To the solid residue was added 1 M cold aqueous hydrochloric acid until the solution had a pH 1˜2. The solid was filtrated and dried in vacuo over night. The solids were treated with diethyl ether (200 mL) and the mixture was ultrasonicated at room temperature for 3 hours and filtered. The solids were treated with 200 mL of diethyl ether and stirred for 2 hours before filtration, which after drying gave 4-(1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yl)-benzoic acid in 33% isolated yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419979B2
Source datasetuspto-grants-2008_09
ORD IDord-d163bcf5d746461b9fed19c0e3ca942f
Source noteuspto-grants-2008_09