Methylamine → (3-Isopropyl-2-propoxybenzyl)methylamine

HRID 1362284Notes

Reaction equation

HRID 1362284 reaction equation
[CH3:1][NH2:2].[CH:3]([C:6]1[C:7]([O:14][CH2:15][CH2:16][CH3:17])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH:9]=O)([CH3:5])[CH3:4].[BH4-].[Na+]>CO>[CH:3]([C:6]1[C:7]([O:14][CH2:15][CH2:16][CH3:17])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9][CH2:1][NH2:2])([CH3:5])[CH3:4]

Participants

5

Procedure

A solution of methylamine (30 mL of a 2.0 M solution in MeOH, 60 mmol) was added to 3-isopropyl-2-propoxybenzaldehyde (1.49 g, 7.22 mmol) and the mixture was stirred for 72 h. The solution was concentrated under reduced pressure. The resulting dark yellow oil was dissolved in EtOH (30 mL) and treated with NaBH4 (0.273 g, 7.22 mmol). After 18 h, the reaction mixture was concentrated under reduced pressure and dissolved in 1 N NaOH (30 mL). The mixture was extracted with Et2O (3×75 mL). The combined organics were dried (Na2SO4) and concentrated to yield the title compound (1.52 g, 95%) as an orange oil: 1H NMR (300 MHz, DMSO-d6) δ 7.21-7.14 (m, 2H), 7.04 (t, J=7.5 Hz, 1H), 3.70 (t, J=6.3 Hz, 2H), 3.63 (s, 2H), 3.32-3.23 (m, 1H), 2.28 (s, 3H), 1.78 (br s, 1H), 1.76-1.71 (m, 2H), 1.16 (d, J=6.9 Hz, 6H), 1.03 (t, J=7.3 Hz, 3H).

Workup

  1. concentrationThe solution was concentrated under reduced pressure
  2. dissolutionThe resulting dark yellow oil was dissolved in EtOH (30 mL)
  3. waitAfter 18 h
  4. concentrationthe reaction mixture was concentrated under reduced pressure
  5. dissolutiondissolved in 1 N NaOH (30 mL)
  6. extractionThe mixture was extracted with Et2O (3×75 mL)
  7. dry with materialThe combined organics were dried (Na2SO4)
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-aa37e502ed5746b6b30249c65238d5c4
Source dataset
uspto-grants-2011_02
Patent number
US07879872B2

Reaction notes

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