Acetic Anhydride → N-(4-Chloro-2-hydroxyphenyl)acetamide
Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[OH:9].[C:10](OC(=O)C)(=[O:12])[CH3:11]>CO>[Cl:8][C:5]1[CH:6]=[CH:7][C:2]([NH:1][C:10](=[O:12])[CH3:11])=[C:3]([OH:9])[CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 2-amino-5-chlorophenol (1.01 g, 7.0 mmol) in methanol (10 mL) was added acetic anhydride (1.08 g, 10.55 mmol) and the reaction mixture was stirred at room temperature for 30 min. The volatiles were removed in vacuo and the residue was purified by silica gel flash chromatography (hexane:ethyl acetate 5:2) to give the subtitled compound (1.19 g).
Aufarbeitung
- customThe volatiles were removed in vacuo
- customthe residue was purified by silica gel flash chromatography (hexane:ethyl acetate 5:2)
Quellen und Nachweise
- ORD-Eintrag
- ord-c24fa62b13a64ab6b70ce5338142fb9d
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07449475B2
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