Reaktion #792144

ord-c76422a8b84f4d1d9c92afd1c17661ec

Reaktionsgleichung

Cl
HCl
Oc1cccc(O)c1
resorcinol
O=C(O)CCc1ccccn1.O=S(=O)(O)O
3-pyridin-2-yl-propionic acid sulphuric acid salt
CC(=O)[O-].[Na+]
NaOAc
O=C(CCc1ccccn1)c1ccc(O)cc1O
final product
Ausbeute 24.0%
O=C(CCc1ccccn1)c1ccc(O)cc1O
1-(2,4-dihydroxyphenyl)-3-(pyridine-2-yl)propan-1-one
Ausbeute 24.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITto stand for 30 min
  2. 2
    Extraktionwas extracted with EtOAc (3×50 ml)
  3. 3
    WaschenThe combined EtOAc layer was washed with water, brine
  4. 4
    Trocknendried over Na2SO4
  5. 5
    SonstigeThe residue obtained
  6. 6
    Sonstigeafter evaporation of the solvent
  7. 7
    Sonstigewas chromatographed over silica gel column
  8. 8
    Sonstigeto give
  9. 9
    workup.ADDITIONmixture of products, which
  10. 10
    Sonstigewas then recrystallized in hot MTBE/Hex

Vorschrift

A mixture of resorcinol (2.2 g, 20 mmol), 3-pyridin-2-yl-propionic acid sulphuric acid salt (5 g, 20 mmol) and 50 ml boron trifluoride diethyl etherate (BF3.Et2O) was stirred at 90 C for 5 hours under N2 (monitored by TLC). The reaction mixture was poured into 10% aqueous NaOAc solution and allowed to stand for 30 min and the solution was neutralized to pH=7 by 1M HCl and was extracted with EtOAc (3×50 ml). The combined EtOAc layer was washed with water, brine and dried over Na2SO4. The residue obtained after evaporation of the solvent was chromatographed over silica gel column using hexane-EtOAc mixture (1:1) as eluent to give mixture of products, which was then recrystallized in hot MTBE/Hex to afford final product (24%) with >97% purity.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09173424B2uspto-grants-2015_11