Sodium Dithionite → AP-24592

HRID 1260813Notes

Reaction equation

HRID 1260813 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][C:10]=2[C:18]([F:21])([F:20])[F:19])[CH2:4][CH2:3]1.S(S([O-])=O)([O-])=O.[Na+].[Na+]>CC(C)=O.O>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][C:10]=2[C:18]([F:21])([F:19])[F:20])[CH2:4][CH2:3]1

Participants

5

Reactant 2

HCID 24489Sodium DithioniteHCID 468389061-Methyl-4-{[4-nitro-2-(trifluoromethyl)phenyl]methyl}piperazine

Product 1

HCID 46838908AP-24592Yield 64.9%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 962WaterSolvent

Procedure

A suspension of 1-methyl-4-(4-nitro-2-(trifluoromethyl)benzyl)piperazine (1.23 g, 4 mmol) and sodium hydrosulfite (7.0 g, 85% pure from Aldrich, 40 mmol) in acetone and water (1:1, 20 mL) was refluxed for 3 h. Upon cooling, the volatile components (mainly acetone) were removed on rotavap, and the resulting mixture was subjected to filtration. The solid was thoroughly washed with EtOAc. The combined filtrate was extracted with n-BuOH (4×), and the combined organic layer was washed with saturated aq. NaHCO3, dried (Na2SO4), filtered, concentrated, and the resulting residue was purified by silica gel chromatography (eluted with 5% MeOH/DCM, MeOH was pre-saturated with ammonia gas) to provide 0.71 g of product as a pale yellow solid.

Workup

  1. temperaturewas refluxed for 3 h
  2. temperatureUpon cooling
  3. customthe volatile components (mainly acetone) were removed on rotavap
  4. filtrationthe resulting mixture was subjected to filtration
  5. washThe solid was thoroughly washed with EtOAc
  6. extractionThe combined filtrate was extracted with n-BuOH (4×)
  7. washthe combined organic layer was washed with saturated aq. NaHCO3
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customthe resulting residue was purified by silica gel chromatography (eluted with 5% MeOH/DCM, MeOH was pre-saturated with ammonia gas)

Sources & evidence

ORD record
ord-0cdcd52ee09d4999a33f117288c02fac
Source dataset
uspto-grants-2013_06
Patent number
US08470851B2

Reaction notes

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