Reaktion #2064693

ord-92f5d6271eb04cd1b57416137c0b4596

Reaktionsgleichung

Cc1ccc(S(=O)(=O)[O-])cc1.c1cc[nH+]cc1
PPTS
[Li][CH2]CCC
n-BuLi
COc1ccc(Br)c(CCC2(c3ccccc3)OCCO2)c1
2-[2-(2-Bromo-5-methoxy-phenyl)-ethyl]-2-phenyl-[1,3]dioxolane
N#Cc1ccc(OCc2ccccc2)cc1
4-benzyloxy-benzonitrile
COc1ccc(C(=O)c2ccc(OCc3ccccc3)cc2)c(CCC(=O)c2ccccc2)c1
3-[2-(4-Benzyloxy-benzoyl)-5-methoxy-phenyl]-1-phenyl-propan-1-one

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto warm to room temperature
  2. 2
    Temperaturrefluxed overnight
  3. 3
    SonstigeThe solution was then quenched with sat. NH4Cl
  4. 4
    Sonstigethe solvent was evaporated
  5. 5
    Temperaturwas refluxed overnight
  6. 6
    SonstigeRegular workup and column purification

Vorschrift

A solution of 2-[2-(2-Bromo-5-methoxy-phenyl)-ethyl]-2-phenyl-[1,3]dioxolane (0.9 g, 2.5 mmol) in 10 ml of dry THF was cooled to −78° C. and n-BuLi (2.5 M in hexane, 1 ml) was added dropwise. The solution was stirred at −78° C. for 2 h and 4-benzyloxy-benzonitrile (0.575 g, 2.75 mmol) in 2 ml of THF was added. The mixture was allowed to warm to room temperature and refluxed overnight. The solution was then quenched with sat. NH4Cl and the solvent was evaporated. A solution of the residue in 20 ml of wet acetone, 5 ml of H2O containing PPTS (188 mg, 0.75 mmol) was refluxed overnight. Regular workup and column purification afforded an unoptimized weight of 0.8 g 3-[2-(4-Benzyloxy-benzoyl)-5-methoxy-phenyl]-1-phenyl-propan-1-one.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06232476B1uspto-grants-2001_05