Diethyl Ether → 1-(6-Chloropyridin-2-yl)propan-1-ol

HRID 932173Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 932173
[Cl:1][C:2]1[N:7]=[C:6]([CH:8]=[O:9])[CH:5]=[CH:4][CH:3]=1.[CH2:10]([Mg]Br)[CH3:11].C(OCC)C>C1COCC1>[Cl:1][C:2]1[N:7]=[C:6]([CH:8]([OH:9])[CH2:10][CH3:11])[CH:5]=[CH:4][CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of 6-chloropicolinaldehyde (1.00 g, 7.06 mmol) in 20 mL of THF at −78° C. was added ethylmagnesium bromide, 3.0 M solution in diethyl ether (3.53 mL, 10.60 mmol) slowly. The reaction mixture was stirred at −78° C. for 2 h. The reaction mixture was quenched with sat'd NH4Cl aqueous solution, and extracted with ether (3×100 mL). The combined organic layers were dried over Na2SO4 and evaporated to provide the crude product. The crude product was purified by chromatography on silica gel, eluting with 10 to 60% EtOAc/hexane to provide the title compound. Mass Spectrum (ESI) m/z=172 (M+1).

Aufarbeitung

  1. customThe reaction mixture was quenched with sat'd NH4Cl aqueous solution
  2. extractionextracted with ether (3×100 mL)
  3. dry with materialThe combined organic layers were dried over Na2SO4
  4. customevaporated
  5. customto provide the crude product
  6. customThe crude product was purified by chromatography on silica gel
  7. washeluting with 10 to 60% EtOAc/hexane

Quellen und Nachweise

ORD-Eintrag
ord-312c872aceed47c7b66e5eb7e7943fb8
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09296736B2

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