Réaction #742249

ord-6341323ae66147b3b237f867cf3338d6

Équation de réaction

CCOC(=O)C=P(c1ccccc1)(c1ccccc1)c1ccccc1
ethoxycarbonylmethylenetriphenylphosphorane
Cc1ccccc1
toluene
CCN(CC)c1ccc(C(C)=O)c(O)c1
1-(4-diethylamino-2-hydroxy-phenyl)ethanone
CCOC(=O)C=C(C)c1ccc(N(CC)CC)cc1O
3(4-Diethylamino-2-hydroxy-phenyl)-but-2-enoic acid ethyl ester

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThen the reaction mixture was heated to reflux
  2. 2
    TempératureAfter refluxing for 31 hours the mixture
  3. 3
    Températurewas cooled down
  4. 4
    Autreevaporated to dryness
  5. 5
    AutreThe resulting dark oil was purified by chromatography
  6. 6
    Autreto yield a colourless oil

Mode opératoire

To a suspension of 5.27 g ethoxycarbonylmethylenetriphenylphosphorane in 10 ml of toluene, a solution of 2.02 g 1-(4-diethylamino-2-hydroxy-phenyl)ethanone (DE 28 44 606) was dropped in at room temperature. Then the reaction mixture was heated to reflux. After refluxing for 31 hours the mixture was cooled down and evaporated to dryness. The resulting dark oil was purified by chromatography to yield a colourless oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE043006E1uspto-grants-2011_12