Benzoyl Peroxide → HCID 19018243, compound
Reaction equation
[CH3:1][C:2]1([CH2:8][O:9][C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.[Br:17]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[CH3:1][C:2]1([CH2:8][O:9][C:10]2[CH:11]=[CH:12][C:13]([CH2:16][Br:17])=[CH:14][CH:15]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2.2 g (10 mmol) of 4-[((1-methyl)cyclohexyl)methoxy]toluene, 1.8 g (10 mmol) of N-bromosuccinimide and 0.02 g of benzoyl peroxide in 60 ml of carbon tetrachloride was refluxed for 16 hours. The reaction was cooled to room temperature, filtered and the filtrate evaporated to give the product which was used without further purification.
Workup
- filtrationfiltered
- customthe filtrate evaporated
- customto give the product which
- customwas used without further purification
Sources & evidence
- ORD record
- ord-ca0abe3162c0455da3dcada0f7ba6584
- Source dataset
- uspto-grants-1994_07
- Patent number
- US05326905
Reaction notes
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