Hydrochloric Acid → Ethyl 4-chloro-2-ethylpyridine-3-carboxylate

HRID 577145Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 577145
Br[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([Cl:13])[CH:5]=[CH:4][N:3]=1.[CH2:14]([Zn]CC)[CH3:15].O.Cl>O1CCOCC1>[Cl:13][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([CH2:14][CH3:15])[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9]

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 59589350Ethyl 2-bromo-4-chloropyridine-3-carboxylateHCID 178418750HCID 178418750, Verbindung

Produkt 1

HCID 19902853Ethyl 4-chloro-2-ethylpyridine-3-carboxylateAusbeute 63 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

Ethyl 2-bromo-4-chloropyridine-3-carboxylate (1.5 g, 5.7 mmol) was dissolved in anhydrous dioxane (45 mL). A solution of diethyl zinc (4.6 mL, 5.1 mmol, 1.1 M in toluene) was added dropwise, and then was added (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium (62 mg, 85 μmol). The mixture was heated at 40° C. overnight, and then water plus 1 N HCl were added. The reaction mixture was extracted 3 times with ethyl acetate. The combined organic phase was washed with brine and dried over sodium sulfate. After evaporation, the residue was dissolved in DCM and purified on silica gel using 0-15% hexane/ethyl acetate to afford ethyl 4-chloro-2-ethylpyridine-3-carboxylate (687 mg, 57% yield).

Aufarbeitung

  1. extractionThe reaction mixture was extracted 3 times with ethyl acetate
  2. washThe combined organic phase was washed with brine
  3. dry with materialdried over sodium sulfate
  4. customAfter evaporation
  5. dissolutionthe residue was dissolved in DCM
  6. custompurified on silica gel using 0-15% hexane/ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-02314bdac21a459cae1c5d07b1787724
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09040538B2

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