Pyridine → 3-Bromo-4-(2'-methylbutyl)benzoic acid 4'-octyloxy-4-biphenylyl ester
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH2:11][CH:12]([CH3:15])[CH2:13][CH3:14])[C:5](Cl)=[O:6].[OH:16][C:17]1[CH:22]=[CH:21][C:20]([C:23]2[CH:28]=[CH:27][C:26]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])=[CH:25][CH:24]=2)=[CH:19][CH:18]=1.N1C=CC=CC=1>C1(C)C=CC=CC=1>[CH2:30]([O:29][C:26]1[CH:27]=[CH:28][C:23]([C:20]2[CH:19]=[CH:18][C:17]([O:16][C:5](=[O:6])[C:4]3[CH:8]=[CH:9][C:10]([CH2:11][CH:12]([CH3:15])[CH2:13][CH3:14])=[C:2]([Br:1])[CH:3]=3)=[CH:22][CH:21]=2)=[CH:24][CH:25]=1)[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This 3-bromo-4-(2'-methylbutyl)benzoic acid chloride (11.5 g, 0.04 mol) was dropwise added to a mixture of 4-hydroxy-4'-octyloxybiphenyl with anhydrous pyridine under ice cooling, followed by agitating the resulting mixture at 50°-60° C. for 2 hours, adding toluene (100 ml), sufficiently agitating the mixture, washing it with 6N-HCl, then with 2N-NaOH aqueous solution and further with water, further drying over anhydrous MgSO4, distilling off toluene and recrystallizing the residue from a mixture of ethanol (100 ml) with ethyl acetate (60 ml) to obtain 3-bromo-4-(2'-methylbutyl)benzoic acid 4'-octyloxy-4-biphenylyl ester (12.2 g), which exhibited liquid crystalline properties and had the following phase transistion points: ##STR45##
Aufarbeitung
- stirringsufficiently agitating the mixture
- washwashing it with 6N-HCl
- dry with materialwith 2N-NaOH aqueous solution and further with water, further drying over anhydrous MgSO4
- distillationdistilling off toluene
- customrecrystallizing the residue
- additionfrom a mixture of ethanol (100 ml) with ethyl acetate (60 ml)
Quellen und Nachweise
- ORD-Eintrag
- ord-ac75e6b686804be3be2e8142ef414ebd
- Quelldatensatz
- uspto-grants-1990_04
- Patentnummer
- US04913838
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