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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727814Generated: November 1, 2026

Water → 2,2-dibutyl-3,4-dihydro-5-(2-quinolylmethoxy)-1(2H)-naphthalenone

https://huagongshe.com/reaction/727814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)quinolineHCID 20394—
ReactantHCID 10659962HCID 10659962—
SolventDimethylformamideHCID 6228—
Product2,2-dibutyl-3,4-dihydro-5-(2-quinolylmethoxy)-1(2H)-naphthalenoneHCID 1054979077.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2,2-dibutyl-3,4-dihydro-5-hydroxy-(2H)-naphthalenone (2.643 g), 2-chloromethylquinoline (1.7 g), and potassium carbonate (1.67 g) in N,N-dimethylformamide (16 ml) was stirred at 80° C. for 4 hours. The cooled mixture was poured into water. The separated oil was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried, and concentrated in vacuo. The crude product was chromatographed on silica gel using 25% ethyl acetate in n-hexane as eluent to yield 2,2-dibutyl-3,4-dihydro-5-(2-quinolylmethoxy)-1(2H)-naphthalenone (3.09 g) as a pale yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045548
Source datasetuspto-grants-1991_09
ORD IDord-7d1c6828d20b464a8b7aad5a7dc2222b
Source noteuspto-grants-1991_09