HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865309Generated: November 1, 2026
Trifluoroacetic acid → HCID 54108731, compound
https://huagongshe.com/reaction/865309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Fluoro-3-methoxybenzoic acid | HCID 3390679 | — |
| Solvent | Trifluoroacetic anhydride | HCID 9845 | — |
| Product | HCID 54108731 | HCID 54108731 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565482 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-5b04758a60b7443e84ec78ce66848981 |
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| Source note | uspto-grants-1996_10 |
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