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Methylamine → HCID 66967533, Verbindung

HRID 1362258
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1362258
[CH3:1][NH2:2].[CH2:3]([O:5][C:6]1[C:13]([O:14][C:15]([F:18])([F:17])[F:16])=[CH:12][CH:11]=[CH:10][C:7]=1[CH:8]=O)[CH3:4].[BH4-].[Na+]>CO>[CH2:3]([O:5][C:6]1[C:13]([O:14][C:15]([F:18])([F:17])[F:16])=[CH:12][CH:11]=[CH:10][C:7]=1[CH2:8][CH2:1][NH2:2])[CH3:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6329MethylamineHCID 4311764Sodium borohydrideHCID 592776102-Ethoxy-3-trifluoromethoxybenzaldehyde

Produkt 1

HCID 66967533HCID 66967533, VerbindungAusbeute 58 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A solution of methylamine (20 mL of a 2.0 M solution if MeOH, 40 mmol) was added to 2-ethoxy-3-trifluoromethoxybenzaldehyde (1.17 g, 4.95 mmol) under N2 and the solution was stirred for 18 h. The solution was concentrated under reduced pressure. The resulting clear oil was dissolved in EtOH (20 mL) and treated with NaBH4 (0.187 g, 4.95 mmol). After stirring for 5.5 h, the reaction mixture was concentrated under reduced pressure, then dissolved in 1 N NaOH (20 mL) and extracted with Et2O (3×50 mL). The combined organics were collected, washed with brine (2×100 mL), dried (Na2SO4) and concentrated to yield the title compound (0.72 g, 58%) as a clear oil: 1H NMR (500 MHz, DMSO-d6) δ 7.40 (dd, J=7.7, 1.55 Hz, 1H), 7.25 (d, J=9.5 Hz, 1H), 7.16 (t, J=7.7 Hz, 1H), 3.97 (t, J=7.0 Hz, 2H), 3.68 (s, 2H), 2.28 (s, 3H), 2.02 (br s, 1H), 1.35-1.30 (m, 3H).

Aufarbeitung

  1. concentrationThe solution was concentrated under reduced pressure
  2. dissolutionThe resulting clear oil was dissolved in EtOH (20 mL)
  3. stirringAfter stirring for 5.5 h
  4. concentrationthe reaction mixture was concentrated under reduced pressure
  5. dissolutiondissolved in 1 N NaOH (20 mL)
  6. extractionextracted with Et2O (3×50 mL)
  7. customThe combined organics were collected
  8. washwashed with brine (2×100 mL)
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-5f5c204f74a84e6192004bcbc6038ad8
Quelldatensatz
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07879872B2

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