Bromine → HCID 131717481, compound
Reaction equation
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([CH:6]=[C:7]2[CH2:12][CH2:11][C:10]([CH3:14])([CH3:13])[CH2:9][C:8]2=[O:15])=[CH:4][CH:3]=1.[Br:18]Br>ClCCl>[Br:18][CH:6]([CH:7]1[CH2:12][CH2:11][C:10]([CH3:14])([CH3:13])[CH2:9][C:8]1=[O:15])[C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:17][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 7.5 °C
Procedure
10 g (0.04 mole) of 2-(4-chlorobenzylidene)-5,5-dimethycyclohexanone prepared according to Example 1(a) were dissolved in 50 ml dichloromethane and cooled to 5-10° C. Bromine (6.4 g, 0.04 mole) was added over 5 minutes to give 2-bromo-2-(α-bromo-4-chlorobenzyl-5,5-dimethylcyclohexanone in solution.
Sources & evidence
- ORD record
- ord-099cc6f1067a484b8995422db853b1e4
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05136081
Reaction notes
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