N-methyl-2-pyrrolidone → 2-(Benzyloxy)-6-butylpyridine

HRID 1471241

Reaktionsgleichung

Reaktionsgleichung von HRID 1471241
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11](Cl)[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN1[CH2:21][CH2:20][CH2:19][C:18]1=O.C([Mg]Br)CCC>O1CCCC1.C/C(/[O-])=C/C(C)=O.C/C(/[O-])=C/C(C)=O.C/C(/[O-])=C/C(C)=O.[Fe+3]>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:18][CH2:19][CH2:20][CH3:21])[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Edukt 3

HCID 13387N-methyl-2-pyrrolidoneHCID 112644642-(Benzyloxy)-6-chloropyridineHCID 178418682HCID 178418682, Verbindung

Produkt 1

HCID 666264812-(Benzyloxy)-6-butylpyridine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 5483663Ferric acetylacetonateKatalysatorHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a flask were added 2.0 g 2-(benzyloxy)-6-chloropyridine, 5.0 ml 1-methyl-2-pyrrolidinone and 50 ml of dry tetrahydrofuran. After cooling to 5 C under nitrogen, 0.16 g iron(III) acetylacetonate were added followed by drop wise addition of 8.5 ml of a 2M solution of butylmagnesium bromide in tetrahydrofuran. After stirring for 1 hour at 22 C, the reaction was cooled to 10 C and quenched with 20 ml aqueous ammonium chloride. The mixture was diluted with water and extracted with hexane. After washing with water and removal of solvent, the product was purified by silica gel chromatography using 10% ethyl acetate in hexane to give 1.6 g of an oil.

Aufarbeitung

  1. temperatureAfter cooling to 5 C under nitrogen
  2. temperaturethe reaction was cooled to 10 C
  3. customquenched with 20 ml aqueous ammonium chloride
  4. additionThe mixture was diluted with water
  5. extractionextracted with hexane
  6. washAfter washing with water and removal of solvent
  7. customthe product was purified by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag
ord-8cdaf24945464d04b5009e0fceeaf351
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09011734B2

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