p-Toluenesulfonic acid → Triphenylphosphine Oxide

HRID 1252628

Reaktionsgleichung

Reaktionsgleichung von HRID 1252628
C1(C)C=CC(S(O)(=O)=[O:8])=CC=1.O[CH:13]([C:16]1[NH:17][CH:18]=[C:19]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:20](=[O:22])[CH:21]=1)OC.[C:31]([CH:36]=[P:37]([C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1)([C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1)([O:33][CH2:34][CH3:35])=[O:32]>O1CCOCC1>[O:22]=[C:20]1[C:19]([O:23][CH2:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[CH:18][NH:17][C:16]([CH:13]=[CH:36][C:31]([O:33][CH2:34][CH3:35])=[O:32])=[CH:21]1.[C:50]1([P:37](=[O:8])([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[C:38]2[CH:39]=[CH:40][CH:41]=[CH:42][CH:43]=2)[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1

Komponenten

6

Versuchsvorschrift

0.5 g of p-toluenesulfonic acid, 6.26 g of 2-(1-hydroxy-1-methoxymethyl)-5-(phenylmethoxy)-4(1H)-pyridinone and 8.35 g of carbethoxymethylenetriphenylphosphorane were stirred for 3 hours in 100 ml of dioxane at 70° C. A clear, dark-colored solution was formed. Evaporation of the solvent in vacuo yielded an oily residue of the title compound and triphenylphosphine oxide. The residue was dissolved in 30 ml of isopropanol and crystals of product began to separate. After standing in a refrigerator overnight, the crystals were filtered off, washed with ether and recrystallized from isopropanol. Yield: 5.72 g, melting point 188° C.

Aufarbeitung

  1. customA clear, dark-colored solution was formed
  2. customEvaporation of the solvent in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a908bb603e0146ed9a83ce1678d4b7aa
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04743685

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