Carbon Dioxide → HCID 21535782, Verbindung
Reaktionsgleichung
[C:1]([O:10]CC)(=O)[C:2]([O:4][C:5]([CH3:8])([CH3:7])[CH3:6])=[O:3].[Li][C:14]#[C:15][CH:16]([CH3:18])[CH3:17].CC(C)C#C.C([Li])CCC.O=O.C(=O)=O>O1CCCC1.O>[CH3:17][CH:16]([CH3:18])[C:15]#[C:14][C:1](=[O:10])[C:2]([O:4][C:5]([CH3:6])([CH3:7])[CH3:8])=[O:3]Komponenten
9
Edukt 6
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Ethyl t-butyl oxalate ##EQU1## can be prepared by the method of Carpino [J. Amer. Chem. Soc. 82: 2725 (1960)], and 1-lithio-3-methylbut-1-yne ##EQU2## can be prepared by reacting commercially available 3-methylbut-1-yne and n-butyllithium under anhydrous conditions in an inert atmosphere (i.e., no H2O, O2, or CO2) at a temperature of from 0° to 5° C. Anhydrous tetrahydrofuran (THF) is the preferred solvent for the reactions of step (a).
Aufarbeitung
- customcan be prepared
- customof from 0° to 5° C
Quellen und Nachweise
- ORD-Eintrag
- ord-51c1aeb0d88d483cafa9e823a224a5b1
- Quelldatensatz
- uspto-grants-1976_05
- Patentnummer
- US03959312
Notizen zur Reaktion
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