Bromine → Methyl 2-(3-bromo-4-hydroxyphenyl)acetate
Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:4][CH:3]=1.[Br:13]Br>C(O)(=O)C>[Br:13][C:7]1[CH:6]=[C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:4]=[CH:3][C:2]=1[OH:1]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methyl 4-hydroxyphenylacetate (10.5 g, 63.0 mmol) was dissolved in acetic acid (200 mL) and the solution was stirred while bromine (150 mL, 0.463 M in acetic acid, 69.5 mmol) was added over 60 minutes. The mixture was stirred overnight and then concentrated by evaporation. Product was purified from the residue over 300 g of silica gel (hexanes/ethyl acetate 5:1) to give methyl 3-bromo-4-hydroxyphenylacetate (11.9 g).
Aufarbeitung
- additionwas added over 60 minutes
- concentrationconcentrated by evaporation
- customProduct was purified from the residue over 300 g of silica gel (hexanes/ethyl acetate 5:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-937ce24930bb41e197b0784c1fb96d06
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09162986B2
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