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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398082Generated: October 30, 2026

Ethyl Bromide → 2-(3-Ethoxyphenyl)-4,5-dihydropyrazolo[1,5-a]quinoline

https://huagongshe.com/reaction/2398082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPhenol, 3-(4,5-dihydropyrazolo(1,5-a)quinolin-2-yl)-HCID 3042689—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Product2-(3-Ethoxyphenyl)-4,5-dihydropyrazolo[1,5-a]quinolineHCID 13412513—

Reaction Steps

2.62 Grams (0.010 mole) of the compound of Example 10 is added to a solution of 0.23 g. (0.010 mole) of sodium in 40 ml. of absolute ethanol at room temperature, then 2.2 g. (0.020 mole) of ethyl bromide is added dropwise. The resulting solution is refluxed for seven hours and allowed to stand overnight at room temperature. After dilution with 30 ml. of water and subsequent evaporation of the ethanol, a residue is obtained which is crystallized from methanol. Yield 2.29 g. of the title compound, m.p. 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024149
Source datasetuspto-grants-1977_05
ORD IDord-5ee4a91051b24501ab41c0447622520e
Source noteuspto-grants-1977_05