Water → 7-Chloro-2H-thieno[2,3-f][1,3]benzodioxole-6-carboxylic acid
Reaktionsgleichung
[OH2:1].[Cl:2][C:3]1[C:4]2[CH:14]=[C:13]3[O:15][CH2:16][O:17][C:12]3=[CH:11][C:5]=2[S:6][C:7]=1[C:8](Cl)=[O:9]>O1CCOCC1>[Cl:2][C:3]1[C:4]2[CH:14]=[C:13]3[O:15][CH2:16][O:17][C:12]3=[CH:11][C:5]=2[S:6][C:7]=1[C:8]([OH:1])=[O:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
40 ml of water are added to a solution of 70 mmol of the compound of Step A in 250 ml of dioxane. After 20 hours' reflux and then return to ambient temperature, a precipitate forms. After filtration and rinsing with water until neutral, the precipitate is dried over P2O5 under reduced pressure, allowing the expecting product to be isolated.
Aufarbeitung
- temperatureAfter 20 hours' reflux
- customreturn to ambient temperature
- filtrationAfter filtration
- washrinsing with water until neutral, the precipitate
- dry with materialis dried over P2O5 under reduced pressure
- customto be isolated
Quellen und Nachweise
- ORD-Eintrag
- ord-7f547cf8cb824ce4b1eb138bd2bd2e6d
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06302837B1
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