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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254827Generated: November 2, 2026

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

https://huagongshe.com/reaction/2254827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
Reactant3-BromoanisoleHCID 16971—
Reactant4-QuinolinecarboxaldehydeHCID 78072—
SolventTetrahydrofuranHCID 8028—
Productalpha-[4-(Benzyloxy)-3-methoxyphenyl]-4-quinolinemethanolHCID 21459134—

Reaction Steps

25 ml of tert.-butylithium 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 numberUS05236952
Source datasetuspto-grants-1993_08
ORD IDord-c5f70cde50974a5ba373f05a4a6e38d8
Source noteuspto-grants-1993_08