Reaktion #46155

ord-770b7d6d1da4405690083fcd544e2270

Reaktionsgleichung

CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester
NO
hydroxyamine
Cl
hydrochloric acid
c1ccncc1
pyridine
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=NO
1-hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carboxylate ethyl ester
Ausbeute 9.5%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with saturated ammonium chloride
  2. 2
    SonstigeThe organic layer obtained
  3. 3
    Extraktionby extracting the reaction mixture with ethyl acetate
  4. 4
    Trocknenwas dried over anhydrous magnesium sulfate
  5. 5
    Einengenconcentrated
  6. 6
    Sonstigethe residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2)

Vorschrift

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester (2 g, 4.85 mmol) and hydroxyamine.hydrochloric acid (1.01 g, 14.6 mmol) were dissolved in pyridine (1.57 ml, 19.4 mmol). The reaction mixture was stirred for 1 hour at 70° C., and washed with saturated ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2) to obtain 1-hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carboxylate ethyl ester (yield 9.5%) as a yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741323B2uspto-grants-2010_06