Hydrogen Bromide → HCID 20392598, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=2)=[CH:8][CH:7]=1)[CH3:2].[Br:22]N1C(=O)CCC1=O.Br>C(Cl)(Cl)(Cl)Cl>[Br:22][CH:5]([C:6]1[CH:11]=[CH:10][C:9]([O:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=2)=[CH:8][CH:7]=1)[C:4]([O:3][CH2:1][CH3:2])=[O:21]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1.17 g of ethyl[p-(p-cyanophenoxy)phenyl]acetate in 20 ml of carbon tetrachloride is added 0.75 g of N-bromosuccinimide and a drop of 48% HBr. The mixture is stirred and refluxed for 42 hours. The solvent is removed under vacuum to give the product.
Workup
- temperaturerefluxed for 42 hours
- customThe solvent is removed under vacuum
- customto give the product
Sources & evidence
- ORD record
- ord-7e35873992934ae1817e428b3397c22d
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04168385
Reaction notes
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