Sodium Hydroxide → 2-(3-Formylphenoxy)-2-methylpropanoic acid
Reaktionsgleichung
[CH:1]([C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[O:6][C:7]([CH3:14])([CH3:13])[C:8]([O:10]CC)=[O:9])=[O:2].[OH-].[Na+]>O1CCOCC1>[CH:1]([C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[O:6][C:7]([CH3:14])([CH3:13])[C:8]([OH:10])=[O:9])=[O:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The obtained Compound 97b (1.0 eq.) was dissolved in 1,4-dioxane, and 1 N NaOH (1.4 eq.) was added thereto. The reaction mixture was stirred at room temperature, and after a volatile material was evaporated, the residual was distributed between methylene chloride and water. An aqueous layer was acidified by using a 12 N HCl and extracted by using methylene chloride. An organic layer was evaporated to obtain Compound 97d.
Aufarbeitung
- customafter a volatile material was evaporated
- extractionextracted
- customAn organic layer was evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-7ab14553e9c542dcad183361b60e0438
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08889881B2
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