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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118854Generated: October 26, 2026

Water → 1-(Quinolin-6-yl)but-1-ene-3-one

https://huagongshe.com/reaction/2118854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant6-QuinolinecarbaldehydeHCID 765653—
SolventDimethyl SulfoxideHCID 679—
Product1-(Quinolin-6-yl)but-1-ene-3-oneHCID 53845647—

Reaction Steps

A mixture of quinoline-6-carboxaldehyde (5.29 g) and 1-triphenylphosphoranylidene-2-propanone (1.5 equiv) in dimethyl sulfoxide (100 ml) was stirred at room temperature for 24 hr. The solution was poured into water (600 ml) which was subsequently extracted with ethyl acetate. The dried (MgSO4) organic fraction was evaporated under reduced pressure and the residue was purified by column chromatography over silica with dichloromethane/ethyl acetate (4:1 v/v) elution to give 1-(quinolin-6-yl)but-1-ene-3-one as a white solid. Pmr spectrum (CDCl3 ; δ in ppm): 2.41 (3H,s); 6.83 (1H,d); 7.3-9.0 (7H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680400
Source datasetuspto-grants-1987_07
ORD IDord-5dac0518cfc3437fa953b7348b5e0324
Source noteuspto-grants-1987_07