Reaktionsgleichung
[C:1]1([S:7]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na].C(O)(C)C.[OH-].[Cu+2:29].[OH-]>O>[CH2:11]([O:10][S:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)(=[O:9])=[O:8])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[Cu:29]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Into a fritted column was added: 12 g (12 meq H+) ion exchange resin (Amberlite® IR 120 brand). Resin beads were washed with 100 ml deionized water. Into a 50 ml beaker were added: 8.6 g (10 meq) sodium dodecyl benzene sulfonate (Biosoft D-40 brand), 7 g water, and 7 g isopropanol. The Biosoft D-40 solution was run through the column and collected in a 100 ml beaker containing: 0.58 g (12 meq Cu) copper hydroxide mixture and 20 g water. The effluent/copper hydroxide mixture was swirl mixed while collecting the effluent. A 10 g water rinse of the column was added to the copper mixture. Extraction of the beaker's contents was done with 2×25 ml toluene. The toluene solubles were dried with molecular sieve. Stripping, on a rotary evaporator removed the toluene, and the resulting solids were vacuum dried overnight at room temperature.
Aufarbeitung
- additionInto a fritted column was added
- washResin beads were washed with 100 ml
- additionInto a 50 ml beaker were added
- customcollected in a 100 ml beaker
- additioncontaining
- customwhile collecting the effluent
- washA 10 g water rinse of the column
- additionwas added to the copper mixture
- extractionExtraction of the beaker's contents
- dry with materialThe toluene solubles were dried with molecular sieve
- customStripping, on a rotary evaporator
- customremoved the toluene
- customdried overnight at room temperature
Quellen und Nachweise
- ORD-Eintrag
- ord-76874a5671d54531a93346002f298ff8
- Quelldatensatz
- uspto-grants-1992_04
- Patentnummer
- US05108500
Verknüpfte Notizen
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