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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-t-Butoxy-3-chloro-2,5,6-trifluoropyridineHCID 10857579—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product4-t-Butoxy-2,3,6-trifluoropyridineHCID 1060854756,470.898%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977133
Source datasetuspto-grants-1999_11
ORD IDord-a114a9ea48c343e39f533457a6f464c2
Source noteuspto-grants-1999_11