Réaction #2006412

ord-0be3c7529c384d788f4e683e69c9c9b8

Équation de réaction

O=S(=O)(Nc1ccc(I)cc1)c1ccccc1
28
O=S(=O)(Nc1ccc(I)cc1)c1ccccc1
4-(Benzenesulfonylamino)-phenyl Iodide
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri-o-tolylphosphine
CCN(CC)CC
Et3N
C=CC(=O)O
acrylic acid
O=C(O)C=Cc1ccc(NS(=O)(=O)c2ccccc2)cc1
title compound 35
Rendement 99.0%
O=C(O)C=Cc1ccc(NS(=O)(=O)c2ccccc2)cc1
3-[4-(Benzenesulfonylamino)-phenyl]-2-propenoic Acid
Rendement 99.0%

Solvants

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe resulting solution was degassed
  2. 2
    Autrepurged several times with N2
  3. 3
    FiltrationThe solution was filtrated through a Celite pad with a fritted glass funnel
  4. 4
    Autrethe filtrate was evaporated
  5. 5
    AutreThe residue was purified by flash chromatography

Mode opératoire

To a solution of 28 (500 mg, 1.39 mmol), in DMF (10 mL) at room temperature were added tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3; 38 mg, 1.67 mmol), tri-o-tolylphosphine (P(o-tol)3, 25 mg, 0.83 mmol), Et3N (483 μL, 3.48 mmol) and finally acrylic acid (84 μL, 1.67 mmol). The resulting solution was degassed and purged several times with N2 then heated overnight at 100° C. The solution was filtrated through a Celite pad with a fritted glass funnel then the filtrate was evaporated. The residue was purified by flash chromatography using CH2Cl2/MeOH (95:5) as solvent mixture yielding the title compound 35 (415 mg, 99%) as yellowish solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE043343E1uspto-grants-2012_05