![](/CAS/20180808/GIF/5465-66-7.gif)
1-(4-bromo-2-nitrophenyl)piperidine synthesis
- Product Name:1-(4-bromo-2-nitrophenyl)piperidine
- CAS Number:5465-66-7
- Molecular formula:C11H13BrN2O2
- Molecular Weight:285.14
![Piperidine](/CAS/GIF/110-89-4.gif)
110-89-4
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364-73-8
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$8.00/10g
![1-(4-bromo-2-nitrophenyl)piperidine](/CAS/20180808/GIF/5465-66-7.gif)
5465-66-7
12 suppliers
$28.60/250mg
Yield:5465-66-7 99%
Reaction Conditions:
with potassium carbonate in (methylsulfinyl)methane at 100;
Steps:
4.1.6. General procedure for the preparation of compounds 11a-g and 12f-g
General procedure: Alkylamine (30mmol) and K2CO3 (4.1g, 30mmol) or CsCO3 (9.8g, 30mmol) was added to compound 10 (10mmol) in DMF or DMSO (20mL). The mixture was heated at 25-120°C for 2-12h. The reaction was diluted with H2O (200mL) and then extracted with EtOAc (200mL×2). The combined organic phases were washed with H2O (200mL×2) and brine (200mL), dried over MgSO4 and concentrated in a vacuum. The residue was purified by flash column chromatography (0-10% EtOAc in petroleum ether).
References:
Li, Jing;Wu, Fangping;Liu, Xingguo;Zou, Yake;Chen, Huixiong;Li, Zheng;Zhang, Lei [European Journal of Medicinal Chemistry,2017,vol. 140,p. 20 - 30]
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110-89-4
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16588-24-2
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$6.00/1g
![1-(4-bromo-2-nitrophenyl)piperidine](/CAS/20180808/GIF/5465-66-7.gif)
5465-66-7
12 suppliers
$28.60/250mg
![Piperidine](/CAS/GIF/110-89-4.gif)
110-89-4
3 suppliers
$15.96/100ML
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55321-64-7
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106-44-5
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$14.00/5g
![1-(4-bromo-2-nitrophenyl)piperidine](/CAS/20180808/GIF/5465-66-7.gif)
5465-66-7
12 suppliers
$28.60/250mg
![Piperidine](/CAS/GIF/110-89-4.gif)
110-89-4
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$15.96/100ML
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33696-00-3
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$10.00/1g
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$5.00/1g
![1-(4-bromo-2-nitrophenyl)piperidine](/CAS/20180808/GIF/5465-66-7.gif)
5465-66-7
12 suppliers
$28.60/250mg
![Piperidine](/CAS/GIF/110-89-4.gif)
110-89-4
3 suppliers
$15.96/100ML
![4-Bromo-2-nitro-1-p-tolyloxy-benzene](/CAS/20180529/GIF/55321-64-7.gif)
55321-64-7
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7697-37-2
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119-33-5
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![1-(4-bromo-2-nitrophenyl)piperidine](/CAS/20180808/GIF/5465-66-7.gif)
5465-66-7
12 suppliers
$28.60/250mg