Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274558Generated: October 25, 2026

Water → alpha-[4-(Benzyloxy)-3-methoxyphenyl]-4-quinolinemethanol

https://huagongshe.com/reaction/274558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-QuinolinecarboxaldehydeHCID 78072—
Reactant1-(Benzyloxy)-4-bromo-2-methoxybenzeneHCID 3613128—
ReactantHCID 178418306HCID 178418306—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Productalpha-[4-(Benzyloxy)-3-methoxyphenyl]-4-quinolinemethanolHCID 21459134—

Reaction Steps

25 ml of tert.-butyllithium solution (1.4M in hexane) are added dropwise at -70° within 10 minutes to 10 g of 4-(benzyloxy)-3-methoxy-bromobenzene dissolved in 100 ml of tetrahydrofuran. After stirring at -70° for 1 hour, 5 g of quinoline-4-carbaldehyde dissolved in 50 ml of tetrahydrofuran are added dropwise within 30 minutes. The reaction mixture is stirred at -40° for 1 hour and at -5° for 1 hour, poured into 200 ml of water and adjusted to pH 4 with glacial acetic acid. The mixture is extracted three times with 50 ml of ether each time. The combined ether phases are washed with water, dried over sodium sulfate and evaporated. There is obtained α-[4-(benzyloxy)-3-methoxyphenyl]-4-quinolinemethanol as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-07070739b3294ad9bb6ed645f6d1076c
Source noteuspto-grants-1995_02