Reaktionsgleichung
[B:1]([OH:4])([OH:3])[OH:2].[OH:5][CH2:6][C@@H:7]([C@H:9]([C@@H:11]([C@@H:13]([CH2:15][OH:16])[OH:14])[OH:12])[OH:10])[OH:8].[CH2:17]([N:21]([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:22][CH2:23][OH:24])[CH2:18][CH2:19][CH3:20]>C1(C)C=CC=CC=1>[CH2:17]([N:21]([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:22][CH2:23][OH:24])[CH2:18][CH2:19][CH3:20].[B:1]([OH:4])([OH:3])[OH:2].[OH:16][CH2:15][C@@H:13]([C@H:11]([C@@H:9]([C@@H:7]([CH2:6][OH:5])[OH:8])[OH:10])[OH:12])[OH:14]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
N,N-dibutylethanolamine/sorbitol borate was prepared as follows. Boric acid (10.3 grams), sorbitol (30.4 grams), and N,N-dibutylethanolamine (28.9 grams) were added to a 250 milliliter flask. One hundred fifty milliliters of toluene was then added. The reaction was allowed to proceed overnight at 110° C., and the byproduct water (˜9 grams) was continuously removed from the reaction by azeotropic distillation. The final solution was evaporated to remove toluene under vacuum, and a yellowish resinous product (˜60 grams) of N,N-dibutylethanolamine/sorbitol borate was obtained.
Aufarbeitung
- customN,N-dibutylethanolamine/sorbitol borate was prepared
- customthe byproduct water (˜9 grams) was continuously removed from the reaction by azeotropic distillation
- customThe final solution was evaporated
- customto remove toluene under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-1a35d7227e84491eabd1d379b726ed47
- Quelldatensatz
- uspto-grants-2003_07
- Patentnummer
- US06585816B1
Verknüpfte Notizen
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