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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409985Generated: October 30, 2026

Trifluoroacetic acid → HCID 69096970, compound

https://huagongshe.com/reaction/2409985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86703302HCID 86703302—
SolventDichloromethaneHCID 6344—
ProductHCID 69096970HCID 6909697092.4%

Reaction Steps

To a solution of tert-butyl [5-chloro-4-methoxy-2-(2-oxo-2-pyridin-3-ylethyl)phenyl]carbamate (1.28 g) in dichloromethane (17 mL) was added trifluoroacetic acid (3.4 mL) under ice-cooling, and the mixture was stirred at room temperature for 24 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and the resulting mixture was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine successively. The organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain the title compound (812 mg). 1H-NMR (CDCl3) δ ppm: 3.95 (3H, s), 6.77-6.85 (1H, m), 7.14 (1H, s), 7.38 (1H, dd, J=4.8, 8.0 Hz), 7.45 (1H, s), 7.86-7.96 (1H, m), 8.36 (1H, br s), 8.53-8.60 (1H, m), 8.90-8.97 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815903B2
Source datasetuspto-grants-2014_08
ORD IDord-6ba0a3cbfae24f62a19aea2c01494bff
Source noteuspto-grants-2014_08