Methane → 2-(Pyridin-4-ylmethoxy)benzaldehyde

HRID 380182Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 380182
[CH:1](=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[OH-].[K+].Cl.[N:13]1[CH:18]=[CH:17][C:16]([CH2:19]Cl)=[CH:15][CH:14]=1.C>CS(C)=O.C(OCC)(=O)C.O>[N:13]1[CH:18]=[CH:17][C:16]([CH2:19][O:4][C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=2[CH:1]=[O:9])=[CH:15][CH:14]=1

Komponenten

8

Versuchsvorschrift

A solution of salicylaldehyde (5 g, 40.9 mmol) in DMSO (75 mL) was treated with crushed potassium hydroxide (5.4 g, 81.8 mmol) and allowed to stir at room temperature for 1 hour. This was then treated with 4-picolyl chloride hydrochloride (6.8 g, 40.9 mmol) and the dark mixture allowed to stir overnight. The mixture was poured into water and extracted twice with ethyl acetate. The combined ethyl acetate extracts were washed with 5% NaOH, three times with water then with brine. Drying over MgSO4 and removal of the solvent under reduced pressure gave the crude product. This was taken up in ethyl acetate, treated with charcoal, filtered, and the solvent removed under reduced pressure to give 5.42 g (62.1%) of the product as an oil; MS-CI 214 (M+1).

Aufarbeitung

  1. stirringto stir overnight
  2. extractionextracted twice with ethyl acetate
  3. washThe combined ethyl acetate extracts were washed with 5% NaOH, three times with water
  4. dry with materialDrying over MgSO4 and removal of the solvent under reduced pressure
  5. customgave the crude product
  6. filtrationfiltered
  7. customthe solvent removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e990cc9022ba4599a03f84423bda0d6f
Quelldatensatz
uspto-grants-2001_10
Patentnummer
US06300501B1

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