Water → 1-(3-Bromo-4-nitrophenyl)-4-methylpiperazine

HRID 2367750Notes

Reaction equation

HRID 2367750 reaction equation
[Br:1][C:2]1[CH:7]=[C:6](F)[CH:5]=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[CH3:12][N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.O>CCOC(C)=O>[Br:1][C:2]1[CH:7]=[C:6]([N:16]2[CH2:17][CH2:18][N:13]([CH3:12])[CH2:14][CH2:15]2)[CH:5]=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10]

Participants

5

Reactant 3

HCID 962WaterHCID 531671-MethylpiperazineHCID 27569932-Bromo-4-fluoro-1-nitrobenzene

Product 1

HCID 117815411-(3-Bromo-4-nitrophenyl)-4-methylpiperazineYield 45%

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

2-Bromo-4-fluoronitrobenzene (949 mg, 4.31 mmol) was added in two portions to neat N-methypiperazine (8 mL) at 0° C. and allowed to warm to room temperature. The reaction was heated to 60° C. for 1 h, and then it was diluted with 50 mL of EtOAc and poured into H2O (50 mL). The layers were separated and the organic layer was washed with satd aq NaHCO3, dried (Na2SO4), and concentrated in vacuo to afford 580 mg (45%) of the title compound as a yellow solid: Mass spectrum (ESI, m/z): Calcd. for C11H14BrN3O2, 300.0 (M+H). found 300.1.

Workup

  1. temperatureThe reaction was heated to 60° C. for 1 h
  2. customThe layers were separated
  3. washthe organic layer was washed with satd aq NaHCO3
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-b7f8859a0e194e058a5d79ec2e5781b2
Source dataset
uspto-grants-2014_04
Patent number
US08697716B2

Reaction notes

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