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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Methoxy-7-(2-methoxyvinyl)quinoline | HCID 68856094 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | HCl tetrahydrofuran | HCID 18422008 | — |
| Product | (6-Methoxyquinolin-7-yl)acetaldehyde | HCID 57682887 | 110% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538123B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-d1df36b1c4154fa78c2805b98af415f7 |
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| Source note | uspto-grants-2009_05 |
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