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ChemicalBook--->CAS DataBase List--->70261-81-3

70261-81-3

70261-81-3 Structure

70261-81-3 Structure
IdentificationBack Directory
[Name]

1-METHYL-4-(4-NITROBENZYL)PIPERAZINE
[CAS]

70261-81-3
[Synonyms]

SKL601
1-(4-Nitrobenzyl)-4-methylpiperazine
1-METHYL-4-(4-NITROBENZYL)PIPERAZINE
1-Methyl-4-(4-nitrobenzyl)piperazine95%
1-Methyl-4-[(4-nitrophenyl)Methyl]piperazine
1-(4-Methyl-3-nitrobenzyl)-4-Methylpiperazine
Piperazine, 1-methyl-4-[(4-nitrophenyl)methyl]-
1-methyl-4-[(4-nitrophenyl)methyl]piperazine-1,4-diium
1-METHYL-4-[(4-NITROPHENYL)METHYL]-PIPERAZINE DIHYDROCHLORIDE
[EINECS(EC#)]

201-215-5
[Molecular Formula]

C12H17N3O2
[MDL Number]

MFCD00976866
[MOL File]

70261-81-3.mol
[Molecular Weight]

235.28
Chemical PropertiesBack Directory
[Boiling point ]

358.2±27.0 °C(Predicted)
[density ]

1.184±0.06 g/cm3(Predicted)
[pka]

7.51±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4-Chloronitrobenzene-->4-Nitrobenzaldehyde-->4-Nitrobenzyl bromide-->Sodium borohydride-->Chloroform
Hazard InformationBack Directory
[Synthesis]

1-Methylpiperazine

109-01-3

4-Nitrobenzaldehyde

555-16-8

1-METHYL-4-(4-NITROBENZYL)PIPERAZINE

70261-81-3

GENERAL PROCEDURE: Acetic acid (AcOH, 100%, 140 mL, 2.44 mol) was added slowly and dropwise over a period of 1 hour to a flask containing sodium hydride (NaBH4, 20.0 g, 0.53 mol) and chloroform (CHCl3, 220 mL) stirred at 0-5° C. The mixture was then stirred for 1.5 hours. The resulting mixture was continued to be stirred at 0-5°C for 1.5 hours. Subsequently, a solution of N-methylpiperazine (28.0 mL, 0.25 mol) and p-nitrobenzaldehyde (43.4 g, 0.26 mol) dissolved in chloroform (60 mL) was added to the above mixture. The reaction mixture was stirred at 0-5°C for 1 hour and then at room temperature for 12 hours. After completion of the reaction, the mixture was treated with distilled water (150 mL) and sodium carbonate (Na2CO3) and the pH was adjusted to 8.0-9.0. The aqueous phase was extracted with ethyl acetate (EtOAc, 2 x 100 mL), the organic layers were combined, washed with distilled water (1 x 100 mL) and dried over anhydrous sodium sulfate (Na2SO4). Filtration and evaporation of the solvent gave 1-methyl-4-(4-nitrophenyl)piperazine (4a) as a pale yellow oil; yield: 61.6 g, 99% yield.

[References]

[1] Tetrahedron Letters, 2012, vol. 53, # 38, p. 5056 - 5058
[2] Russian Journal of Organic Chemistry, 2013, vol. 49, # 4, p. 563 - 567
[3] Zh. Org. Khim., 2013, vol. 49, # 4, p. 580 - 584
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 21, p. 8801 - 8815
[5] Russian Journal of Organic Chemistry, 2011, vol. 47, # 10, p. 1556 - 1563
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