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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535474Generated: October 29, 2026

Ammonia → 6-Isopropyl-3-pyridazinone

https://huagongshe.com/reaction/535474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3-Methyl-2-butanoneHCID 11251—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
ReactantAminoammonium hydroxideHCID 44558531—
SolventWaterHCID 962—
Product6-Isopropyl-3-pyridazinoneHCID 23028147—
Product4-Hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-oneHCID 59549140—

Reaction Conditions

Temperature120 °C

Reaction Steps

7.1 A mixture of 14.4 g (157 mmol) of glyoxylic acid monohydrate and 50 ml (464 mmol) of isopropyl methyl ketone is heated at 120° C. with stirring for two hours. The reaction mixture is cooled to 40° C., and 70 ml of water and 12 ml of 32% aqueous ammonia solution are added. This mixture is extracted three times with dichloromethane. 7.55 ml (155 mmol) of hydrazinium hydroxide are added to the aqueous phase, and the mixture is heated at reflux for 18 hours. The reaction mixture is cooled to room temperature and extracted with dichloromethane. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on a silica-gel column with petroleum ether/tert-butyl methyl ether as eluent, giving 4-hydroxy-5,5,6-trimethyl-4,5-dihydro-2H-pyridazin-3-one as colourless crystals (ESI 157) and 6-isopropyl-2H-pyridazin-3-one as colourless crystals (ESI 139).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859547B2
Source datasetuspto-grants-2014_10
ORD IDord-f56c9d1cab244069952015e3015a6c08
Source noteuspto-grants-2014_10