Ethylene carbonate → Bis-alpha-naphthyl-(4-[2-hydroxy-ethoxy]-2-hydroxy-phenyl)-triazine

HRID 8345

Reaktionsgleichung

Reaktionsgleichung von HRID 8345
C(=O)([O-])[O-].[K+].[K+].[C:7]1(=O)[O:11][CH2:10][CH2:9][O:8]1.[C:13]1([C:23]2[N:28]=[N:27][N:26]=[C:25]([C:29]3[CH:34]=[CH:33]C(O)=[CH:31][C:30]=3[OH:36])[C:24]=2[C:37]2[C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[CH:40]=[CH:39][CH:38]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1>CN(C=O)C>[C:13]1([C:23]2[N:28]=[N:27][N:26]=[C:25]([C:29]3[CH:34]=[CH:33][C:7]([O:11][CH2:10][CH2:9][OH:8])=[CH:31][C:30]=3[OH:36])[C:24]=2[C:37]2[C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[CH:40]=[CH:39][CH:38]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

9.39 g of potassium carbonate and 4.39 g of ethylene carbonate are added to 20 g of the product from Example A6 in 200 ml of anhydrous DMF. The reaction mixture is heated at 140° C. for 18 h. The salts which precipitate are filtered off and washed with toluene. The combined organic phase is freed of solvent in vac. and used directly for the further reaction.

Aufarbeitung

  1. filtrationThe salts which precipitate are filtered off
  2. washwashed with toluene
  3. customand used directly for the further reaction

Quellen und Nachweise

ORD-Eintrag
ord-5ff40fbc24cd473c904d9efe22b51f9b
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07087753B2

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