Bromine → 2-Phenyl-6-nitrobenzyl bromide
Reaktionsgleichung
[C:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:8]=2[CH3:16])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:17]Br>C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[C:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:8]=2[CH2:16][Br:17])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The procedure of Example 8 was employed, except that the starting material was 2 g of 2-phenyl-6-nitrotoluene which was reacted with 1.5 g of bromine and 0.110 g of benzoyl peroxide. In this way, 2 g (77% yield) of yellowish crystals were recovered.
Quellen und Nachweise
- ORD-Eintrag
- ord-d1e4f62367514b188bb2362884fc3a3c
- Quelldatensatz
- uspto-grants-1992_08
- Patentnummer
- US05135838
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