Reaktion #5998

ord-f93f0562c268458cb7f1687b9cb17055

Reaktionsgleichung

O
water
CC[O-].[Na+]
sodium ethoxide
CCOC(=O)C(NC(C)=O)C(=O)OCC
diethyl acetamidomalonate
COc1cccc(CCl)c1OCc1ccccc1
benzyl chloride
COc1cccc(CCl)c1OCc1ccccc1
3-(Chloromethyl)-2-phenylmethoxyanisole
CCOC(=O)C(Cc1cccc(OC)c1OCc1ccccc1)(NC(C)=O)C(=O)OCC
pure crystalline product
Ausbeute 66.4%
CCOC(=O)C(Cc1cccc(OC)c1OCc1ccccc1)(NC(C)=O)C(=O)OCC
2-(Acetylamino)-2-[[3-methoxy-2-(phenylmethoxy) -phenyl]methyl]-propanedioic acid, diethyl ester
Ausbeute 66.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture is heated
  2. 2
    Temperaturat reflux for 2 hours
  3. 3
    SonstigeThe supernatant is decanted from the separated gum
  4. 4
    workup.DISSOLUTIONThe gum is dissolved in 2 L of ether
  5. 5
    Trocknenthe solution dried (magnesium sulfate)
  6. 6
    Einengenconcentrated to ca 300 mL volume

Vorschrift

A quantity of 136.20 g (0.42 mole) of 21 wt.% sodium ethoxide in ethanol is added to a stirred solution of 90.14 g (0.415 mole) of diethyl acetamidomalonate (Aldrich) in 800 mL of absolute ethanol. A solution of the benzyl chloride derivative of Example 38 in 500 mL of absolute ethanol is added and the mixture is heated at reflux for 2 hours. The cooled mixture is poured into 4 L of ice and water containing 20.0 g of glacial acetic acid. The supernatant is decanted from the separated gum. The gum is dissolved in 2 L of ether, the solution dried (magnesium sulfate), and concentrated to ca 300 mL volume. Petroleum ether (100 mL) is added to precipitate 107.1 g (66.4% yield) of pure crystalline product; mp 94°-96° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246943uspto-grants-1993_09