![](/CAS/20150408/GIF/1132940-59-0.gif)
3-BroMo-5-(tert-butyl)-4-Methoxyaniline synthesis
- Product Name:3-BroMo-5-(tert-butyl)-4-Methoxyaniline
- CAS Number:1132940-59-0
- Molecular formula:C11H16BrNO
- Molecular Weight:258.15
![1-BroMo-3-(tert-butyl)-2-Methoxy-5-nitrobenzene](/CAS/20150408/GIF/1132940-55-6.gif)
1132940-55-6
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![3-BroMo-5-(tert-butyl)-4-Methoxyaniline](/CAS/20150408/GIF/1132940-59-0.gif)
1132940-59-0
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Yield:1132940-59-0 100%
Reaction Conditions:
with hydrogen;5 % platinum on sulfided carbon in methanol; for 3 h;
Steps:
1.H
[00502] Part H. Preparation of tert-butyl 3-bromo-5-tert-butyl-4-methoxyphenylcarbamate.; [00503] A solution ofthe product from Part G (960mg, 3.33mmol) in methanol (17mL) was treated with5 % platinum on sulfided carbon (lOOmg), followed by hydrogenation under balloon pressure for 3h, and then filtered through celite and concentrated under vacuum to afford the 3-bromo-5-tert-butyl-4- methoxyaniline as a yellow oil (860mg, 3.33mmol, 100%). A solution of this material in THF (17mL) was treated with di-tert-butyl dicarbonate (800mg, 3.66mmol) followed by warming at reflux for 2h.Concentration under vacuum afforded a beige solid, which was purified by silica gel column chromatography eluting with EtOAc/hexanes. Solid was triturated with hexanes, collected by filtration, and dried under vacuum to give the title compound as a nearly white solid (890mg, 75 %).
References:
WO2009/39134,2009,A1 Location in patent:Page/Page column 105