Hydrochloric Acid → 2-(4-(2-Hydroxyethyl)phenoxy)acetaldehyde
Reaktionsgleichung
Cl.C([O:4][CH:5](OCC)[CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][OH:16])=[CH:10][CH:9]=1)C>O1CCOCC1.O>[OH:16][CH2:15][CH2:14][C:11]1[CH:12]=[CH:13][C:8]([O:7][CH2:6][CH:5]=[O:4])=[CH:9][CH:10]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Concentrated hydrochloric acid (5 mL) was added to a solution of 2-(4-(2,2-diethoxyethoxy)phenyl)ethanol (example 3, step a) (0.76 g) in 1,4-dioxane (10 mL) and the resulting mixture was stirred for 1 h. The reaction was diluted with water (50 mL) and extracted with ethyl acetate (3×50 mL). The combined organic solutions were washed with water (50 mL) and brine (50 mL), then dried over sodium sulphate, filtered and evaporated in vacuo to give the subtitled compound, which was used directly. Yield 0.35 g.
Aufarbeitung
- extractionextracted with ethyl acetate (3×50 mL)
- washThe combined organic solutions were washed with water (50 mL) and brine (50 mL)
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customevaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-a2b29d693f394fa28aee0d86ea005683
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08148373B2
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