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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057727Generated: October 25, 2026

Water → 1-(3-Chlorophenoxy)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1057727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-ChlorophenolHCID 7933—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product1-(3-Chlorophenoxy)-4-(4-pyridylmethyl)phthalazineHCID 22742020—

Reaction Steps

Under exclusion of air, 200 mg (0.78 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine (Example 67A.1), 173 mg (1.25 mmol) K2CO3, and 120 mg (0.94 mmol) 3-chlorophenol (Fluka) are heated in 2 ml DMSO for 3 h to 90° C. The reaction mixture is distributed between 20 ml water and 20 ml ethyl acetate, and the aqueous phase separated and extracted with 2 portions of ethyl acetate. The organic phase is washed with water and brine, dried (MgSO4), and concentrated by evaporation. The residue is dissolved in ≈15 ml THF, precipitated with hexane, and filtered. Title compound is obtained from the evaporated filtrate after chromatography (SiO2; ethyl acetate/CH3OH, 4:1): m.p.: 143-145° C.; HPLC: tRet(Grad20-100)=8.9; FAB MS (M+H)+=348.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514974B2
Source datasetuspto-grants-2003_02
ORD IDord-dfceb4f6ec5a4e408cfb319ae210130d
Source noteuspto-grants-2003_02