HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 59398226 | HCID 59398226 | — |
| Product | (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde | HCID 59398313 | — |
Reaction Steps
Into 3 mL of a 90% aqueous trifluoroacetic acid solution, 156 mg of 1-(1,3-dioxolan-2-ylmethyl)-4-chloroquinolin-2(1H)-one was dissolved, and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, and the reaction mixture was alkalified with an aqueous saturated sodium hydrogen carbonate solution, and then extracted with ethyl acetate. The organic layer 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 192 mg of a pale yellow oily substance, (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524738B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-4a786edb6cba4750b7f60d17b93ce9d9 |
| Source note | uspto-grants-2013_09 |