1-Bromo-2-methylpropane → HCID 67276389, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][NH2:10])=[C:4]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:3]=1.[H-].[Na+].Br[CH2:18][CH:19]([CH3:21])[CH3:20]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][NH:10][CH2:18][CH:19]([CH3:21])[CH3:20])=[C:4]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:3]=1Participants
4
Procedure
In a manner analogous to example 1 c, the process is carried out by a reaction of 4 g (16 mmol) of (4-bromo-2-tert-butylphenyl)ethylamine (example 1b) with 1.4 g (34 mmol) of 60% sodium hydride and with 3.7 ml (34 mmol) of 1-bromo-2-methylpropane. 1.5 g of (4-bromo-2-tert-butylphenyl)ethylisobutylamine are obtained in the form of an oil (yield=30%).
Sources & evidence
- ORD record
- ord-7747337ac40544be8b6dba637e52f9e9
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163952B2
Reaction notes
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