[(3-Methoxypropyl)(methyl)amino]acetonitrile → (2-Aminoethyl)(3-methoxypropyl)methylamine

HRID 1669197Notes

Reaction equation

HRID 1669197 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][N:6]([CH2:8][C:9]#[N:10])[CH3:7]>[Ni].CCO>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][N:6]([CH3:7])[CH2:8][CH2:9][NH2:10]

Participants

4

Procedure

A mixture of nitrile 273 (1.94 g, 14.0 mmol), cNH3 (8 mL) and Raney Nickel (50% slurry in water, 5.3 g) in EtOH (100 mL) was stirred under H2 (60 psi) for 4 h. The mixture was filtered through Celite, washed with EtOH (50 mL) and the solvent was evaporated to give crude diamine 274 (1.65 g, 83%) as a yellow oil, which was used without further purification: 1H NMR δ 3.42 (t, J=6.4 Hz, 2H, CH2N), 3.33 (s, 3H, OCH3), 2.76 (t, J=6.1 Hz, 2H, CH2), 2.43 (t, J=7.2 Hz, 2H, CH2), 2.40 (t, J=6.2 Hz, 2H, CH2), 2.21 (s, 3H, NCH3), 1.74 (tt, J=7.2, 6.2 Hz, 2H, CH2), NH2 not observed; MS (APCI) m/z 147 (MH+, 100%); HRMS calcd for C7H18N2O (M+) m/z 146.1419, found 146.1424.

Workup

  1. filtrationThe mixture was filtered through Celite
  2. washwashed with EtOH (50 mL)
  3. customthe solvent was evaporated

Sources & evidence

ORD record
ord-86a994fe6a7645079bd917dbb7c2fdb5
Source dataset
uspto-grants-2011_08
Patent number
US07989451B2

Reaction notes

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