HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385502Generated: October 29, 2026
Trifluoroacetic acid → (2-oxo-1,8-naphthyridin-1(2H)-yl)acetaldehyde
https://huagongshe.com/reaction/385502
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-(1,3-dioxolan-2-ylmethyl)-1,8-naphthyridin-2(1H)-one | HCID 57815206 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-oxo-1,8-naphthyridin-1(2H)-yl)acetaldehyde | HCID 57815222 | 84.1% |
Reaction Steps
To 1.1 g of 1-(1,3-dioxolan-2-ylmethyl)-1,8-naphthyridin-2(1H)-one, 11 mL of a 90% aqueous trifluoroacetic acid solution was added, and the mixture was stirred at room temperature for 2 hours. Then, 1.1 mL of water was added thereto and the mixture was stirred for 13 hours, and thereto was further added 1.1 mL of water and the mixture was stirred for 3 hours 30 minutes, and stirred at 50 to 70° C. for 1 hour 30 minutes. The solvent was distilled off under reduced pressure, and to the resultant residue, a saturated aqueous sodium hydrogen carbonate solution, water and chloroform were added. 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 with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.75 g of (2-oxo-1,8-naphthyridin-1(2H)-yl)acetaldehyde as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367831B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-bd2ab88a4a9042339d93c64539b1d88b |
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| Source note | uspto-grants-2013_02 |
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