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Benzyl Alcohol → 2-Benzyloxy-6-cyano-3-methylpyridine

HRID 1243812
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1243812
Br[C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([C:9]#[N:10])[N:3]=1.[CH2:11]([OH:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[H-].[Na+]>O1CCCC1.C(OCC)(=O)C>[CH2:11]([O:18][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([C:9]#[N:10])[N:3]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 244Benzyl AlcoholHCID 24758Sodium hydrideHCID 219283226-Bromo-5-methylpyridine-2-carbonitrile

Produkt 1

HCID 219283052-Benzyloxy-6-cyano-3-methylpyridineAusbeute 52 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel
HCID 8857
Ethyl Acetate
Lösungsmittel

Versuchsvorschrift

To a solution of 2-bromo-6-cyano-3-methylpyridine (272 mg) and benzyl alcohol (156 mg) in tetrahydrofuran (20 mL) was added sodium hydride (40 mg), and the mixture was heated under reflux for one hour. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed successively with saturated aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. After removal of the sodium sulfate by filtration, the organic solvent was evaporated off in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=19:1) to give the title compound (161 mg) as a colorless liquid.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for one hour
  3. washwashed successively with saturated aqueous sodium bicarbonate and saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customAfter removal of the sodium sulfate
  6. filtrationby filtration
  7. customthe organic solvent was evaporated off in vacuo
  8. customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate=19:1)

Quellen und Nachweise

ORD-Eintrag
ord-049107b3004541678c41d2d7cd3017b8
Quelldatensatz
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07119107B2

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