Water → 4-(N-cyclohexyl-N-methylaminomethyl)aniline

HRID 1870521Notes

Reaction equation

HRID 1870521 reaction equation
[CH:1]1([N:7]([CH3:18])[CH2:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][CH:10]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.B.[Na].O>CO.[Ni](Br)Br>[CH:1]1([N:7]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][CH:10]=2)[CH3:18])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

6

Procedure

To a solution of N-cyclohexyl-N-methyl-N-(4-nitrobenzyl)amine (12.4 g, 50.0 mmol) in methanol (250 ml) were added nickel bromide (1.09 g, 5.0 mmol) and then sodium boron hydride (7.57 g, 200 mmol) at 0° C., and the mixture was stirred at room temperature for 30 minutes. To the mixture were added nickel bromide (0.55 g, 2.5 mmol) and then sodium boron hydride (3.78 g, 100 mmol) at 0° C., and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture was added water (100 ml), and the mixture was concentrated under reduced pressure. To the residue was added ethyl acetate, and insoluble material was filtered off with Celite. The filtrate was washed with ethyl acetate, and the ethyl acetate layer was dried with MgSO4 and concentrated under reduced pressure. The residue was washed with hexane to give 4-(N-cyclohexyl-N-methylaminomethyl)aniline (3.99 g, 37%).

Workup

  1. concentrationthe mixture was concentrated under reduced pressure
  2. additionTo the residue was added ethyl acetate, and insoluble material
  3. filtrationwas filtered off with Celite
  4. washThe filtrate was washed with ethyl acetate
  5. dry with materialthe ethyl acetate layer was dried with MgSO4
  6. concentrationconcentrated under reduced pressure
  7. washThe residue was washed with hexane

Sources & evidence

ORD record
ord-7c8ba11468fa4b79b7704a2f78da9308
Source dataset
uspto-grants-2000_08
Patent number
US06096780

Reaction notes

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