Reaktionsgleichung
[CH2:1]([C:8]1[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=1[CH2:10]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BrH:16]>>[CH2:1]([C:8]1[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=1[CH2:10][Br:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
3
Versuchsvorschrift
2-Benzylbenzyl alcohol (commercial) (1 g) was suspended in 48% aqueous hydrobromic acid (10 ml) and stirred vigorously for 20 hours. The resultant suspended solid was extracted twice with hexane and the extracts dried (MgSO4) and evaporated to give 2-benzyl benzylbromide as yellow solid (1.3 g, 98%).
Aufarbeitung
- extractionwas extracted twice with hexane
- dry with materialthe extracts dried (MgSO4)
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-93f2795254ed44abb88915047391a63e
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05834468
Verknüpfte Notizen
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