Reaktion #1850

ord-daea2679130c4e96a69efc91647c4537

Reaktionsgleichung

Cc1ccc(O)c(I)n1
3-hydroxy-2-iodo-6-methylpyridine
CC(=O)[O-].[K+]
potassium acetate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
C=CC(=O)OCC
ethyl acrylate
C=C(C(=O)OCC)c1nc(C)ccc1O
Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled
  2. 2
    Filtrationfiltered
  3. 3
    workup.ADDITIONadded to water (100 ml)
  4. 4
    ExtraktionThe product was extracted into ethyl acetate (3×30 ml)
  5. 5
    WaschenThe combined extracts were washed with water (2×25 ml) and with brine (25 ml)
  6. 6
    Trocknendried over sodium sulphate
  7. 7
    Sonstigeevaporated
  8. 8
    workup.WAITThis left a tan solid

Vorschrift

To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726315uspto-grants-1998_03