Reaktionsgleichung
[CH2:1]([OH:18])[CH:2]([OH:17])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[B:19]([OH:22])([OH:21])[OH:20].O>C1(C)C=CC=CC=1>[B:19]([OH:22])([OH:21])[OH:20].[CH2:1]([OH:18])[CH:2]([OH:17])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Approximately 86 g of 1,2-hexadecanediol and approximatel 200 g toluene solvent was charged to a 1 liter reactor equipped with agitator, heater and Dean- Stark tube with condenser. The contents were heated up to 80°-90° C. to dissolve the diol and approximately 11 g boric acid was added. The mixture was heated up to 155° C. until water evolution stopped over a period of 4 hours. Approximately 9 ml water was removed by azeotropic distillation. The solvent was removed by vacuum distillation and the product was filtered at 100° C. through diatomaceous earth. The product became waxy after cooling.
Aufarbeitung
- customequipped with agitator, heater and Dean- Stark tube with condenser
- temperatureThe contents were heated up to 80°-90° C.
- additionwas added
- customApproximately 9 ml water was removed by azeotropic distillation
- customThe solvent was removed by vacuum distillation
- filtrationthe product was filtered at 100° C. through diatomaceous earth
- temperatureafter cooling
Quellen und Nachweise
- ORD-Eintrag
- ord-201666d346c349dea9321610c777aff7
- Quelldatensatz
- uspto-grants-1988_11
- Patentnummer
- US04788340
Verknüpfte Notizen
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