HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600995Generated: October 25, 2026
4-t-Butoxy-3-chloro-2,5,6-trifluoropyridine → 4-t-Butoxy-2,3,6-trifluoropyridine
https://huagongshe.com/reaction/1600995
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-t-Butoxy-3-chloro-2,5,6-trifluoropyridine | HCID 10857579 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-t-Butoxy-2,3,6-trifluoropyridine | HCID 10608547 | 56,470.898% |
Reaction Steps
To 4-t-butoxy-3-chloro-2,5,6-trifluoropyridine (24.92 g, 0.104 mmol) in 100 mL of methanol was added 2.5 g of Pearlman's catalyst (Aldrich Chemical Co.), and the mixture was stirred at ambient temperature for 14 hours under and atmosphere of hydrogen. An additional 2.5 g of catalyst was added, and the mixture was stirred for another 22 hours. The mixture was filtered, the filtrate was concentrated, and the residue was extracted with hexane/ether. After filtration, the solvent was removed by evaporation, and the residue was purified by flash chromatography (ethyl acetate:hexane 1:16) to yield 12.05 g of 4-t-butoxy-2,3,6-trifluoropyridine. MS 206 (M+H)+, 233 (M+18)+ ; 1H NMR (CDCl3)∂: 1.52 (s, 9H), 6.5 (m, 1H); 19F NMR (CDCl3, CFCl3 as reference)∂: 72.60 (dd, J1 =14.3, J2 =21.0 Hz), 89.74 (dd, J1 =14.3, J2 =21.0 Hz), 164.68 (dt, J1 =4.2, J2 =21.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977133 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-a114a9ea48c343e39f533457a6f464c2 |
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| Source note | uspto-grants-1999_11 |
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