Benzoyl Peroxide → HCID 54060551, compound

HRID 262204Notes

Reaction equation

HRID 262204 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([Cl:19])[CH:13]=1.[Br:20]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][Br:20])=[C:14]([Cl:19])[CH:13]=1

Participants

5

Reactant 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 54519170HCID 54519170, compound

Product 1

HCID 54060551HCID 54060551, compound

Reagents, catalysts & solvents 1

HCID 5943Carbon TetrachlorideSolvent

Procedure

4-(2-Chloro-4-methoxystyryl)-2-chlorobenzyl bromide was prepared from 27.8 g. of 2,3'-dichloro-4-methoxy-4'-methylstilbene, 17.8 g. of N-bromosuccinimide and 0.5 g. of benzoyl peroxide in carbon tetrachloride according to the procedure of Example 10(b); yield 23.0 g., m.p. 106°-108° C.

Sources & evidence

ORD record
ord-6eecd795c87d4083a1b814d199d49457
Source dataset
uspto-grants-1979_05
Patent number
US04153719

Reaction notes

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