Reaktion #65945

ord-d7fb85277acc4ce09961ab0718ced4f2

Reaktionsgleichung

CC(=O)[O-]
acetate
[Na]
sodium
CCC=O
propanal
CO
methanol
COc1ccc(F)c2c1CC(N)CO2
3-amino-8-fluoro-5-methoxychroman
CCCN(CCC)C1COc2c(F)ccc(OC)c2C1
3-Dipropylamino-8-fluoro-5-methoxychroman

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeIn a round-bottom flask equipped with a magnetic stirrer
  2. 2
    FiltrationThe solution was filtered through Celite
  3. 3
    Sonstigethe solvent was evaporated
  4. 4
    Sonstigeto leave a liquid residue which
  5. 5
    Extraktionextracted with ether (2×100 mL)
  6. 6
    TrocknenThe collected ether phases were dried (K2CO3)
  7. 7
    Filtrationfiltered
  8. 8
    Einengenconcentrated in vacuo

Vorschrift

In a round-bottom flask equipped with a magnetic stirrer were placed the crude acetate of 3-amino-8-fluoro-5-methoxychroman (1.18 g; approx. 3.9 mmol) from above, dry methanol (10 mL), propanal (2.8 mL; 39 mmol), glacial acid (pH 3-4) and sodium boronhydride (0.25 g; 3.9 mmol) but with no molecular sieves. The reaction mixture was stirred under nitrogen at room temperature for 1 h. The solution was filtered through Celite and the solvent was evaporated to leave a liquid residue which was diluted with water (25 mL) and extracted with ether (2×100 mL) after adjusting pH to 10-11 with 5M sodium hydroxide. The collected ether phases were dried (K2CO3), filtered and concentrated in vacuo.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420151uspto-grants-1995_05