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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193098Generated: October 31, 2026

Trifluoroacetic acid → (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde

https://huagongshe.com/reaction/2193098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59398226HCID 59398226—
Product(4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-6a9b386908e647458a8eadf4556e3913
Source noteuspto-grants-2012_12