Bromine → 2-Phenyl-6-nitrobenzyl bromide
Reaction equation
[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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Sources & evidence
- ORD record
- ord-12d1792f5354429e8ed21fb7c34db631
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05200544
Reaction notes
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