Sulfuric Acid → 4-Benzyl-2-(chloromethyl)morpholine

HRID 1598364

Reaktionsgleichung

Reaktionsgleichung von HRID 1598364
[CH2:1]([N:8]([CH2:12][CH:13]([OH:16])[CH2:14][Cl:15])[CH2:9][CH2:10]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)(O)O>[OH-].[Na+]>[CH2:1]([N:8]1[CH2:9][CH2:10][O:16][CH:13]([CH2:14][Cl:15])[CH2:12]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

To 3-benzyl-6-chloro-3-azahexane-1,5-diol (164 g) was added dropwise under ice-cooling over 30 minutes conc. sulfuric acid (205 ml, 1.99 mol) in the absence of a solvent and allowed to rise to room temperature and stirred for 25 minutes. The reaction mixture was heated at 150° C. for 45 minutes. After cooling, ice-water (1000 ml) was added to the reaction mixture under ice-cooling and then 50% aqueous sodium hydroxide (1000 ml) was added dropwise over one hour. After insolubles were filtered off, the filtrate was extracted with chloroform (1000 ml×3). The organic layer was washed successively with purified water (1000 ml) and a saturated aqueous solution of sodium chloride (1000 ml), dried over potassium carbonate and the solvent was distilled off under reduced pressure. The residue was chromatographed over silica gel and the fraction from ethyl acetate-hexane (1/6) gave 4-benzyl-2-chloromethylmorpholine (107.25 g) as a colorless oil. A total yield of the two steps=72%.

Aufarbeitung

  1. customto rise to room temperature
  2. temperatureAfter cooling
  3. temperaturecooling
  4. filtrationAfter insolubles were filtered off
  5. extractionthe filtrate was extracted with chloroform (1000 ml×3)
  6. washThe organic layer was washed successively with purified water (1000 ml)
  7. dry with materiala saturated aqueous solution of sodium chloride (1000 ml), dried over potassium carbonate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customThe residue was chromatographed over silica gel

Quellen und Nachweise

ORD-Eintrag
ord-4f099be6cd414842b7674b05fdcfb929
Quelldatensatz
uspto-grants-1998_04
Patentnummer
US05736550

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