Ethanol → Benzeneacetic acid, 3,5-dibromo-4-hydroxy-, ethyl ester
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][C:11]([OH:13])=[O:12])[CH:5]=[C:6]([Br:9])[C:7]=1[OH:8].S(=O)(=O)(O)O.[CH2:19](O)[CH3:20]>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][C:11]([O:13][CH2:19][CH3:20])=[O:12])[CH:5]=[C:6]([Br:9])[C:7]=1[OH:8]Komponenten
4
Versuchsvorschrift
3,5-Dibromo-4-hydroxyphenylacetic acid (60 g, 0.19 mol), from Preparation A, was suspended in 1 L of ethanol and 10 mL of concentrated sulfuric acid and heated at reflux overnight. The reaction mixture was cooled, concentrated and the product collected by filtration, washed with water, and dried in a vacuum oven to obtain ethyl 3,5-dibromo-4-hydroxyphenylacetate.
Aufarbeitung
- temperatureat reflux overnight
- temperatureThe reaction mixture was cooled
- concentrationconcentrated
- filtrationthe product collected by filtration
- washwashed with water
- customdried in a vacuum oven
Quellen und Nachweise
- ORD-Eintrag
- ord-bddfa451827142e3b0ae96b43ddcd2e1
- Quelldatensatz
- uspto-grants-1994_02
- Patentnummer
- US05284971
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