Toluene → Diethenyl benzene-1,4-dicarboxylate
Reaktionsgleichung
[C:1]([OH:12])(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH:13]#[CH:14].[C:15]1(C)C=CC=C[CH:16]=1>[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Re].[Re]>[C:1]([O:12][CH:13]=[CH2:14])(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH:15]=[CH2:16])=[O:7])=[CH:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 8.0 g of terephthalic acid (48 mmol), 0.10 g of Re2(CO)10 (0.15 mmol) and 17.3 g of toluene was subjected to vinylation at 140° C., a nitrogen pressure of 2 bar and an acetylene pressure of 18 bar for 6 h. Divinyl terephthalate was obtained, which was detectable by means of GC-MS analysis.
Aufarbeitung
- customwas subjected to vinylation at 140° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-cdb6101b28e64e3fb355e06235d710be
- Quelldatensatz
- uspto-grants-2011_10
- Patentnummer
- US08044233B2
Notizen zur Reaktion
Wird geladen…