Réaction #968884

ord-897d363fadf64e2dadeca438c9f29a34

Équation de réaction

CCOC(=O)C(C(=O)OCC)C1SC=CN1C(=O)OCC
product
CCOC(=O)C(C(=O)OCC)C1SC=CN1C(=O)OCC
Diethyl 2-(3-(ethoxycarbonyl)-2,3-dihydrothiazol-2-yl)malonate
O=C1C(=O)C(Cl)=C(Cl)C(Cl)=C1Cl
tetrachloro-1,2-benzoquinone
CCOC(=O)C(C(=O)OCC)=C1NC=CS1
title compound
CCOC(=O)C(C(=O)OCC)=C1NC=CS1
Diethyl 2-(thiazol-2(3H)-ylidene)malonate

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewas then washed with saturated aqueous sodium bicarbonate solution (200.0 ml) and brine (100.0 ml)
  2. 2
    SéchageThe organic layer was dried over MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    Concentrationconcentrated in vacuum
  5. 5
    Autrethe crude product was purified by flash column chromatography on silica gel

Mode opératoire

To a solution of the product of Example 44A (12.9 g, 40.7 mmoles) in dichloromethane (100.0 ml) was added tetrachloro-1,2-benzoquinone (10.0 g, 40.7 mmoles) in portions at about 0° C., such that the mixture always had time to decolorize to a yellow-orange color. The mixture was then stirred for about 1 hour at 0° C. and was then washed with saturated aqueous sodium bicarbonate solution (200.0 ml) and brine (100.0 ml). The organic layer was dried over MgSO4, filtered, concentrated in vacuum and the crude product was purified by flash column chromatography on silica gel using hexanes/ethyl acetate (2:1) as the mobile phase to provide the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08993632B2uspto-grants-2015_03