Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963708Generated: 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/963708

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 numberUS05763489
Source datasetuspto-grants-1998_06
ORD IDord-de5fa2d55fc147be8f2cf1834edada49
Source noteuspto-grants-1998_06