N-bromobutanimide → HCID 77230413, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6].[Br:14]N1C(=O)CCC1=O>>[Br:14][CH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6]Participants
3
Procedure
The subtitle compound was prepared from ethyl 3,5-dimethylbenzoate (2 g) and N-bromosuccinimide (2 g) by the method of example 5 step (i). Purification was by chromatography eluting with 5% ethyl acetate in isohexane Yield 1.85 g.
Workup
- customPurification
- washeluting with 5% ethyl acetate in isohexane Yield 1.85 g
Sources & evidence
- ORD record
- ord-d916d26fce2248df95e7ccae945b7faf
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06200981B1
Reaction notes
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