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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344041Generated: October 30, 2026

2-(5-Methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl bromide → 2-[2-(5-methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl]-6-diphenylmethyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/344041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-Methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl bromideHCID 10563876—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant6-diphenylmethyl-3(2H)-pyridazinoneHCID 54323769—
SolventDimethylformamideHCID 6228—
Product2-[2-(5-methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl]-6-diphenylmethyl-3(2H)-pyridazinoneHCID 7018619083%

Reaction Steps

To a solution of 6-diphenylmethyl-3(2H)-pyridazinone (0.22 g) and potassium tert-butoxide (0.10 g) in N,N-dimethylformamide (2 ml) was added a solution of 2-(5-methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl bromide (0.18 g) in N,N-dimethylformamide (3 ml) at room temperature. The reactIon mixture was stirred for 2 hours at the same temperature and partitioned between water and ethyl acetate. The organic layer was washed with water (3 times) and brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed (n-hexane - ethyl acetate) over silica gel to afford 2-[2-(5-methoxy-1,2,3,4-tetrahydro-1-naphthyl)ethyl]-6-diphenylmethyl-3(2H)-pyridazinone (0.25 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05863918
Source datasetuspto-grants-1999_01
ORD IDord-4ae3722097b746ffbd50f2f47a61e9a9
Source noteuspto-grants-1999_01