Reaktionsgleichung
[CH:1]1[C:6]([C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)=[CH:5][CH:4]=[C:3](O)[CH:2]=1.C(OC1C=CC(C(Cl)=O)=CC=1)CCCCCCC.[CH2:33]([O:41][C:42]1[CH:50]=[CH:49][C:45]([C:46]([OH:48])=[O:47])=[CH:44][CH:43]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40].Cl>N1C=CC=CC=1>[CH2:33]([O:41][C:42]1[CH:43]=[CH:44][C:45]([C:46]([OH:48])=[O:47])=[CH:49][CH:50]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40].[OH:13][C:10]1[CH:9]=[CH:8][C:7]([C:6]2[CH:1]=[CH:2][CH:3]=[CH:4][CH:5]=2)=[CH:12][CH:11]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
11.2 g (0.06 mol) of p,p'-biphenol and 5.4 g (0.02 mol) of 4-octyloxybenzoyl chloride derived from 4-octyloxybenzoic acid were dissolved in 100 ml of dried pyridine, which were stirred at room temperature for a night. After the completion of the reaction, the reaction mixture was added with 6 normal hydrochloric acid to adjust pH to not more than 1 and then the precipitate was taken out by filtration. Thus obtained precipitate was recrystallized from ethanol to obtain 4.4 g (yield: 53%) of a white crystal.
Aufarbeitung
- customAfter the completion of the reaction
- filtrationthe precipitate was taken out by filtration
- customThus obtained precipitate was recrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-a17d1b3421094bbfb8e3d101338174fa
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05211879
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