Reaktion #42760

ord-f0f1881db2bf48f9b8fc7269f3cdc6c7

Reaktionsgleichung

O
water
COc1ccc(COc2ccc(C(C)=O)c(O)c2)cc1
1-[2-Hydroxy-4-(4-methoxy-benzyloxy)-phenyl]-ethanone
CCN(CC)CC
Triethylamine
CC(C)C(=O)Cl
Isobutyryl chloride
COc1ccc(COc2ccc(C(C)=O)c(OC(=O)C(C)C)c2)cc1
Isobutyric acid 2-acetyl-5-(4-methoxy-benzyloxy)-phenyl ester

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile warming to room temperature
  2. 2
    Sonstigethe dichloromethane layer is separated
  3. 3
    Waschenwashed with saturated brine (100 ml)
  4. 4
    Trocknendried (MgSO4)
  5. 5
    workup.ADDITIONtreated with activated charcoal (300 mg)
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigeevaporated
  8. 8
    Sonstigeto give a pale pink solid

Vorschrift

1-[2-Hydroxy-4-(4-methoxy-benzyloxy)-phenyl]-ethanone (9.11 g, 0.034 mol) is dissolved in dry dichloromethane (120 ml) under an atmosphere of dry argon. Triethylamine (5.14 ml, 0.037 mol) and 4-dimethylaminopyridine (0.204 g, 1.67 mmol) are added, and the mixture is cooled to 0° C. using an ice-water bath. Isobutyryl chloride (3.89 ml, 0.037 mol) is then added dropwise, and the mixture is stirred while warming to room temperature. The mixture is poured into water (100 ml), and the dichloromethane layer is separated, washed with saturated brine (100 ml), dried (MgSO4), treated with activated charcoal (300 mg), filtered and evaporated to give a pale pink solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732435B2uspto-grants-2010_06