HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636005Generated: October 29, 2026
Trifluoroacetic anhydride → 2-Propoxy-5-iodonicotinic acid
https://huagongshe.com/reaction/1636005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | N-Iodosuccinamide | HCID 21864724 | — |
| Reactant | HCID 22648221 | HCID 22648221 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-Propoxy-5-iodonicotinic acid | HCID 11638094 | — |
Reaction Steps
N-Iodosuccinamide (18.22 g, 0.08 mol), trifluoroacetic acid (100 ml) and trifluoroacetic anhydride (25 ml) were added to 2-propoxynicotinic acid (0.054 mol). The mixture was refluxed for 2.5h, cooled and the solvents evaporated. The residue was extracted from water with ethyl acetate and the organics washed with water (twice) and brine (twice), dried (MgSO4) and concentrated. The red residue was redissolved in ethyl acetate washed with sodium thiosulfate solution (twice), water (twice), brine (twice), redried (MgSO4) and concentrated to give the desired product as a solid; 1H NMR (300 MHz, CDCl3): δ=1.05 (t, 3H), 1.85-2.0 (m, 2H), 4.5 (t, 2H), 8.5 (s, 1H), 8.6 (s, 1H), Analysis: found C, 35.16; H, 3.19; N, 4.46. Calcd for C9H10INO3: C, 35.19; H, 3.28; N, 4.56%; LRMS (TSP): 529.5 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06512002B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-ba038c7575684903abe6852b473072f4 |
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| Source note | uspto-grants-2003_01 |
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