Boron tribromide → 3-Hydroxy-5-(trifluoromethyl)benzonitrile
Reaktionsgleichung
C[O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1)[C:6]#[N:7].B(Br)(Br)Br>ClCCl>[OH:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:10]=1)[C:6]#[N:7]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-methoxy-5-(trifluoromethyl)benzonitrile (1.30 g, 6.46 mmol) in dry dichloromethane (30 mL) was added BBr3 (0.0920 mL, 0.969 mmol) at 0° C. The reaction mixture was stirred at rt for two days, quenched with 10% sodium bicarbonate (50 mL) and extracted with DCM (2×200 mL). Combined organic portions were dried over anhydrous sodium sulphate and concentrated to afford the title product (1.1 g).
Aufarbeitung
- customquenched with 10% sodium bicarbonate (50 mL)
- extractionextracted with DCM (2×200 mL)
- dry with materialCombined organic portions were dried over anhydrous sodium sulphate
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-80907c91cea8495eb61eee847f100761
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer
- US08975400B2
Notizen zur Reaktion
Wird geladen…