Triethylamine → 5-Ethoxycarbonyl-2-methoxy-2-oxo-1,3,2-benzo-dioxaphosphole
Reaktionsgleichung
C(N(CC)CC)C.[OH:8][C:9]1[CH:10]=[C:11]([CH:17]=[CH:18][C:19]=1[OH:20])[C:12]([O:14][CH2:15][CH3:16])=[O:13].[P:21](Cl)(Cl)([O:23][CH3:24])=[O:22]>CCOCC>[CH2:15]([O:14][C:12]([C:11]1[CH:17]=[CH:18][C:19]2[O:20][P:21]([O:23][CH3:24])(=[O:22])[O:8][C:9]=2[CH:10]=1)=[O:13])[CH3:16]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Triethylamine (2.211 g, 21.86 mM) was added to a solution of 1.989 g (10.93 mM) of ethyl 3,4-dihydroxybenzoate in 30 ml of ether. The mixture was cooled to -30° C. to -20° C. and a solution of 1.627 g (10.93 mM) of methyl dichlorophosphate in 10 ml of ether was added thereto dropwise with stirring over 10 minutes. The reaction mixture was stirred at the same temperature for 5 minutes, the bath was then removed and the temperature was allowed to rise to 20° C. Filtration and washing were carried out by the procedure of Reference Example 1, and the filtrate and washings were concentrated at room temperature (20°~25° C.) under reduced pressure. There was obtained 2.387 g (84.6% yield) of 5-ethoxycarbonyl-2-methoxy-2-oxo-1,3,2-benzo-dioxaphosphole as a viscous oil.
Aufarbeitung
- temperatureThe mixture was cooled to -30° C. to -20° C.
- stirringThe reaction mixture was stirred at the same temperature for 5 minutes
- customthe bath was then removed
- customto rise to 20° C
- filtrationFiltration
- washwashing
- concentrationthe filtrate and washings were concentrated at room temperature (20°~25° C.) under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-cabb5ab605c64d3ea3581d183779e73e
- Quelldatensatz
- uspto-grants-1989_01
- Patentnummer
- US04801703
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