Reaktion #4569

ord-92c9585a51c84d6bac68d122a75409e7

Reaktionsgleichung

O=C(O)Cc1ccc(C(=O)c2ccccc2)cc1[N+](=O)[O-]
2-nitro-4-benzoylphenylacetic acid
CCN(CC)CC
triethylamine
CCOC(=O)Cl
ethylchloroformate
COCCOC
1,2-dimethoxyethane
CCOC(=O)Cc1ccc(C(=O)c2ccccc2)cc1[N+](=O)[O-]
ethyl 2-nitro-4-benzoylphenylacetate
Ausbeute 94.0%

Reaktionsbedingungen

Temperatur
10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction
  2. 2
    SonstigeThe organic phase was separated
  3. 3
    Trocknendried over magnesium sulfate
  4. 4
    Einengenconcentrated to an oil, which
  5. 5
    Sonstigeto crystallize

Vorschrift

To a solution of 13.8 g. (48.4 mmoles) of 2-nitro-4-benzoylphenylacetic acid in 150 ml. of 1,2-dimethoxyethane at 15° C. was added 5.87 g. (58.1 mmole) of triethylamine. After 5 minutes 5.75 g. (53.2 mmoles) of ethylchloroformate was added and the reaction mixture allowed to stir at 10° C. for 15 minutes. Ethanol (15 ml.) was added and the reaction subsequently was added to a mixture of diethyl ether and a saturated brine solution. The organic phase was separated, dried over magnesium sulfate and concentrated to an oil, which was induced to crystallize, 14.3 g. (94% yield), m.p. 61°-62° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725616uspto-grants-1988_02