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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503215Generated: October 31, 2026

3,4-bis(benzyloxy)-6-[(E)-2-phenylvinyl]pyridazine → HCID 178515965, compound

https://huagongshe.com/reaction/1503215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-bis(benzyloxy)-6-[(E)-2-phenylvinyl]pyridazineHCID 117691127—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 178515965HCID 17851596540.2%

Reaction Steps

To a solution (8 mL) of 3,4-bis(benzyloxy)-6-[(E)-2-phenylvinyl]pyridazine (272 mg) in ethanol was added 10% palladium-carbon (90 mg), and the mixture was stirred under a hydrogen atmosphere at room temperature for 4 hr. The catalyst was filtered off through celite, and the filtrate was concentrated under reduced pressure. To the residue was added ethyl acetate-chloroform, and the resulting solid was collected by filtration and dried under reduced pressure to give 3-hydroxy-6-(2-phenylethyl)pyridazin-4(1H)-one (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212147B2
Source datasetuspto-grants-2015_12
ORD IDord-2fb10f5d39a34dfe9109ef2017eb1a83
Source noteuspto-grants-2015_12