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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865309Generated: November 1, 2026

Trifluoroacetic acid → HCID 54108731, compound

https://huagongshe.com/reaction/865309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Fluoro-3-methoxybenzoic acidHCID 3390679—
SolventTrifluoroacetic anhydrideHCID 9845—
ProductHCID 54108731HCID 5410873132%

Reaction Steps

A solution of 2-fluoro-3-methoxyphenyl)-3-oxo-propanoic acid from Step 1 (1.96 g, 8.6 mmol) in 4 mL of trifluoroacetic acid and 2 mL of trifluoroacetic anhydride was stirred at room temperature for 1 hour. The solution was concentrated in vacuo, the residue dissolved in ether, and the ethereal solution was washed with saturated aqueous NaHCO3, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to give a solid that was purified by flash chromatography to provide 0.37 g (32%) of the desired ketone. The aqueous phase from the NaHCO3 was acidified, extracted with ether, washed with brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo to provide 1.13 g, of recovered 2-fluoro-3-methoxyphenyl)-3-oxo-propanoic acid: mp 112°-118° C.; 1H NMR (CDCl3 /300 MHz) 7.86 (dd, J=8.66, 1.41 Hz, 1H), 7.00 (apparent t, J=8.26 Hz, 1H), 4.96 (s, 2H), 4.31 (S, 2H), 3.97 (S, 3H); 19F NMR (CDCl3 /282 MHz) -142.2 (d). Mass spectrum M+ =196.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565482
Source datasetuspto-grants-1996_10
ORD IDord-5b04758a60b7443e84ec78ce66848981
Source noteuspto-grants-1996_10