Methylamine → HCID 59277580, compound

HRID 1362264Notes

Reaction equation

HRID 1362264 reaction equation
[CH3:1][NH2:2].[CH2:3]([O:6][C:7]1[C:14]([O:15][C:16]([F:19])([F:18])[F:17])=[CH:13][CH:12]=[CH:11][C:8]=1[CH:9]=O)[CH2:4][CH3:5].[BH4-].[Na+]>CO>[CH3:1][NH:2][CH2:9][C:8]1[CH:11]=[CH:12][CH:13]=[C:14]([O:15][C:16]([F:19])([F:18])[F:17])[C:7]=1[O:6][CH2:3][CH2:4][CH3:5]

Participants

5

Procedure

A solution of methylamine (19 mL of a 2.0 M solution in MeOH, 38 mmol) was added to 2-propoxy-3-trifluoromethoxybenzaldehyde (1.15 g, 4.60 mmol). The mixture was stirred for 18 h. The solution was concentrated under reduced pressure. The resulting clear oil was dissolved in EtOH (19 mL) and treated with NaBH4 (0.174 g, 4.60 mmol). After stirring for 5.5 h, the reaction mixture was concentrated under reduced pressure, then dissolved in 1 N NaOH (19 mL). The mixture was extracted with Et2O (3×50 mL). The organics were collected, washed with brine (2×100 mL), dried (Na2SO4) and concentrated to yield the title compound (0.89 g, 73%) as an orange oil: 1H NMR (300 MHz, DMSO-d6) δ 7.41 (dd, J=7.7, 1.6 Hz, 1H), 7.25 (dd, J=6.7, 1.3 Hz, 1H), 7.16 (t, J=7.7 Hz, 1H), 3.87 (t, J=6.3 Hz, 2H), 3.68 (s, 2H), 2.27 (s, 3H), 2.07 (br s, 1H), 1.74 (q, J=6.4 Hz, 2H), 1.02 (t, J=3.1 Hz, 3H).

Workup

  1. concentrationThe solution was concentrated under reduced pressure
  2. dissolutionThe resulting clear oil was dissolved in EtOH (19 mL)
  3. stirringAfter stirring for 5.5 h
  4. concentrationthe reaction mixture was concentrated under reduced pressure
  5. dissolutiondissolved in 1 N NaOH (19 mL)
  6. extractionThe mixture was extracted with Et2O (3×50 mL)
  7. customThe organics were collected
  8. washwashed with brine (2×100 mL)
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-1e49c290dc2c4a6eaf41cd8ed5f3681a
Source dataset
uspto-grants-2011_02
Patent number
US07879872B2

Reaction notes

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