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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494968Generated: October 25, 2026

6-Methoxy-7-(2-methoxyvinyl)quinoline → (6-Methoxyquinolin-7-yl)acetaldehyde

https://huagongshe.com/reaction/494968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-7-(2-methoxyvinyl)quinolineHCID 68856094—
SolventEthyl AcetateHCID 8857—
SolventHCl tetrahydrofuranHCID 18422008—
Product(6-Methoxyquinolin-7-yl)acetaldehydeHCID 57682887110%

Reaction Conditions

Temperature70 °C

Reaction Steps

1.41 g of 6-methoxy-7-(2-methoxyvinyl)quinoline was dissolved in 40 ml of 2 N hydrochloric acid-tetrahydrofuran (1:1), and the obtained mixture was then stirred at 70° C. for 2 hours. The reaction solution was cooled to a room temperature. It was diluted with ethyl acetate and then washed with a saturated sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution. The organic layer was dried over magnesium sulfate and then concentrated under a reduced pressure, so as to obtain 1.45 g of (6-methoxyquinolin-7-yl)acetaldehyde containing triphenylphosphine oxide. This compound was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-d1df36b1c4154fa78c2805b98af415f7
Source noteuspto-grants-2009_05