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

HRID 2097030
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HRID 2097030 반응식
[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]
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참가 물질

5

반응물 3

HCID 6329MethylamineHCID 4311764Sodium borohydrideHCID 592776233-Isopropyl-2-propoxybenzaldehyde

생성물 1

HCID 66966658(3-Isopropyl-2-propoxybenzyl)methylamine수율 95%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-faf887179cc74b1c9b4c01ff6371219d
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450307B2

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