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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297403Generated: October 29, 2026

Sulfuric Acid → 4-ethyl-6-methoxy-2H-phthalazin-1-one

https://huagongshe.com/reaction/2297403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[2-(4,4-Dimethyl-4,5-dihydro-oxazol-2-yl)-5-methoxy-phenyl]-propan-1-oneHCID 10611435—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-ethyl-6-methoxy-2H-phthalazin-1-oneHCID 1838161144%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1-[2-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-5-methoxy-phenyl]-propan-1-one (6.4 g, 15.9 mmoles), prepared as described in example 8, in 110 ml of a mixture of water (10 ml), ethanol (100 ml) and concentrated H2SO4 (8 ml) up to 200 ml with ethanol, was stirred under N2 and reflux for 20 hours, then concentrated, taken up in water and extracted more times with ethyl ether. The organic phases were washed with water, anhydrified and brought to dryness to give an oil which was dissolved in acetic acid and added, at 15° C., with hydrazine monohydrate (1.56 g, 31.2 mmoles) in acetic acid (10 ml). At the end of the addition, the mixture was heated to 80° C. and, after 20 hours, brought to small volume, taken up in water, neutralised with NaHCO3 and extracted more times with CHCl3. The organic phases were anhydrified and brought to dryness to give a residue, which was flash chromatographed (eluent: hexane/ethyl acetate 9:1, then 7:3). There were thus obtained 1.34 g of the title compound (yield: 44%). m.p.: 230-235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492360B1
Source datasetuspto-grants-2002_12
ORD IDord-0d27123532c94966872832facbcf990c
Source noteuspto-grants-2002_12