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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256720Generated: October 31, 2026

Potassium Carbonate → 6-[4-(3-hydroxypropyloxy)phenyl]-5-methyl-4,5-dihydro-3(2H)-pyridazinone

https://huagongshe.com/reaction/256720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-1-propanolHCID 12308—
Reactant6-(4-Hydroxyphenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-oneHCID 135542478—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-[4-(3-hydroxypropyloxy)phenyl]-5-methyl-4,5-dihydro-3(2H)-pyridazinoneHCID 15682642—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 361 mg (1.62 mmol) of the THP-derivative of 3-bromo-1-propanol prepared above, 220 mg (1.08 mmol) of 6-(4-hydroxyphenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone and 298 mg (2.15 mmol) of powdered anhydrous potassium carbonate in 3 ml of DMF is heated at 100° C. for 2 hr. After cooling the reaction mixture is diluted with 25 ml of water and extracted with EtOAc (3×25 ml). The combined organic extracts are washed once with water, dried (MgSO4), filtered, and the solvent removed under vacuum. The residue is taken up in 5 ml of methanol, about 200 mg of pyridinium p-toluenesulfonate added, and the mixture heated at 60° C. for 2 hr under N2. The solvent is removed under vacuum and the residue is flash chromatographed on silica gel (95:5 CHCl3 :CH3OH) to give 252 mg of 6-[4-(3-hydroxypropyloxy)phenyl]-5-methyl-4,5-dihydro-3(2H)-pyridazinone as a white solid. 1H-NMR (CDCl ): δ1.18 (d, 3H); 1.83 (t, 1H); 2.00 (quintuplet, 2H); 2.40 (d, 1H); 2.63 (d pair, 1H); 3.25 (m, 1H); 3.80 (m, 2H); 4.10 (t, 2H); 6.90 (d, 2H); 7.63 (d, 2H); 8.65 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258519
Source datasetuspto-grants-1993_11
ORD IDord-68781b8311244c7d901fa867315e97a7
Source noteuspto-grants-1993_11