Butyl-2,3-epoxypropyl ether → Bis-alpha-naphthyl-(2-hydroxy-4-[3-n-butoxy-2-hydroxy-propoxy]-phenyl)-triazine

HRID 8343

Reaktionsgleichung

Reaktionsgleichung von HRID 8343
C([CH:5]1[O:17][CH:6]1[CH2:7][O:8][CH2:9][CH:10]1O[CH:11]1[CH2:12]CCC)CCC.[C:18]1([C:28]2[N:33]=[N:32][N:31]=[C:30]([C:34]3[CH:39]=[CH:38][C:37]([OH:40])=[CH:36][C:35]=3[OH:41])[C:29]=2[C:42]2[C:51]3[C:46](=[CH:47][CH:48]=[CH:49][CH:50]=3)[CH:45]=[CH:44][CH:43]=2)[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1>[Br-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C.C1(C)C(C)=CC=CC=1>[C:18]1([C:28]2[N:33]=[N:32][N:31]=[C:30]([C:34]3[CH:39]=[CH:38][C:37]([O:40][CH2:5][CH:6]([OH:17])[CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH3:12])=[CH:36][C:35]=3[OH:41])[C:29]=2[C:42]2[C:51]3[C:46](=[CH:47][CH:48]=[CH:49][CH:50]=3)[CH:45]=[CH:44][CH:43]=2)[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1

Komponenten

5

Edukt 2

HCID 86596549Butyl-2,3-epoxypropyl etherHCID 136338648Bis-alpha-naphthyl-(2,4-dihydroxyphenyl)-triazine

Produkt 1

HCID 136338647Bis-alpha-naphthyl-(2-hydroxy-4-[3-n-butoxy-2-hydroxy-propoxy]-phenyl)-triazine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 73727Phosphonium, ethyltriphenyl-, bromide (1:1)KatalysatorHCID 7237O-XyleneLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

6.60 g of butyl-2,3-epoxypropyl ether and 0.78 g of ethyl-triphenyl-phosphonium bromide are added to a solution of 20.0 g of the product from Example A6 in 200 ml of xylene. That reaction mixture is heated to boiling for 18 h. 0.5 g of activated carbon is then added to the reaction mixture and the resulting mixture is stirred at 25° C. for 1 h. After filtration of the reaction mixture on Hyflo® (kieselguhr; Fluka 56678), the solvent is removed in vac. Chromatography of the residue on silica gel yields the product of melting point: 118–119° C.

Aufarbeitung

  1. temperatureThat reaction mixture is heated
  2. addition0.5 g of activated carbon is then added to the reaction mixture
  3. filtrationAfter filtration of the reaction mixture on Hyflo® (kieselguhr; Fluka 56678)
  4. customthe solvent is removed in vac
  5. customChromatography of the residue on silica gel yields the product of melting point: 118–119° C.

Quellen und Nachweise

ORD-Eintrag
ord-47a2ac6edb95468782048df6afee6428
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07087753B2

Verknüpfte Notizen

Wird geladen…