HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193060Generated: November 2, 2026
Trifluoroacetic acid → (7-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde
https://huagongshe.com/reaction/2193060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-(1,3-Dioxolan-2-ylmethyl)-7-methoxyquinolin-2(1h)-one | HCID 59398178 | — |
| Product | (7-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde | HCID 59397833 | — |
Reaction Steps
To 0.56 g of 1-(1,3-dioxolan-2-ylmethyl)-7-methoxyquinolin-2(1H)-one, 5.6 mL of a 90% aqueous trifluoroacetic acid solution was added, the mixture was stirred at room temperature for 2 hours. The solvent was removed under reduced pressure, water and chloroform was added thereto, and the reaction mixture was adjusted to pH 7.0 with an aqueous saturated sodium hydrogen carbonate solution and stirred for 2 hours. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.36 g of a yellow oily substance, (7-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329694B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-e34977aafc8548a997be1ebe04cd5406 |
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| Source note | uspto-grants-2012_12 |
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