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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418928Generated: November 1, 2026

1-Methoxyphthalazine → HCID 44239509, compound

https://huagongshe.com/reaction/2418928

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethoxyphthalazineHCID 154882—
Reactant3-IodooxetaneHCID 13356686—
ReagentHydrogen PeroxideHCID 784—
ReagentSulfuric AcidHCID 1118—
CatalystCID 516917HCID 516917—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 44239509HCID 4423950934%

Reaction Conditions

Temperature60 °C

Reaction Steps

H2O2 (30% in H2O; 0.23 mL, 2.25 mmol) was added dropwise over 5 min to a stirred solution of 1-methoxyphthalazine 1l (120 mg, 0.75 mmol), concentrated H2SO4 (80 μL, 1.5 mmol), 3-iodooxetane (276 mg, 1.5 mmol) and iron(II) sulfate heptahydrate (63 mg, 0.225 mmol) in DMSO (7.5 mL) at 60 °C. After 1-2 min a further portion of iron(II) sulfate heptahydrate (50 mg, 0.19 mmol) was added and the mixture was stirred at 60 °C for 60 min. Ater allowing to cool, the mixture was poured into a 0.2 M solution of NaOH which has been saturated with solid NaCl (40 mL) and EtOAc (50 mL). The aqueous and organic layers were partitioned and the aqueous layer was extracted with EtOAc (1 x 30 mL). The combined organic extracts were dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude residue. The residue was purified by column chromatography on silica gel using EtOAc / hexanes (0:1 to 3:2) to give the desired product 2l (54 mg, 34%) as a solid. An analytical sample was triturated with Et2O / EtOAc for data purposes.

Provenance & Evidence

DOI10.1021/jo9010624
Source datasetMinisci dataset from Roche
ORD IDord-3b08d7848aae4d6da08ad8bfcd983910
Source noteMinisci dataset from Roche