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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648106Generated: October 25, 2026

Tribromoacetaldehyde → 2-(Bromomethyl)-6-methoxyquinoline

https://huagongshe.com/reaction/1648106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTribromoacetaldehydeHCID 8256—
ReactantEthyl AcetateHCID 8857—
Reactant6-MethoxyquinaldineHCID 70648—
CatalystPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product2-(Bromomethyl)-6-methoxyquinolineHCID 2161804330.6%

Reaction Steps

A solution of 10 g (57.7 mmol) of 6-methoxy-2-methylquinoline and 30 drops of pyridine in 40 mL of N,N-dimethylformamide was stirred at 60° C. while a solution of 16.21 g (57.7 mmol) of tribromoacetaldehyde in 20 mL of N,N-dimethylformamide was added over 15 min. The reaction mixture was stirred for another 2 hr and then cooled and poured onto 600 mL of ice-water. Work-up with ethyl acetate was carried out in the usual manner. The crude product was purified by flash chromatography on 800 g of silica gel, eluting with hexane-ethyl acetate (4:1) afforded 4.45 g (30.6%) of the title compound as a violet solid. An analytical sample was obtained by recrystallization from ethanol to give colorless crystals, mp 103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434186
Source datasetuspto-grants-1995_07
ORD IDord-05f640d1166041ebbf0d4aa9e957cf61
Source noteuspto-grants-1995_07