Triethylamine → HCID 25179430, Verbindung

HRID 2101262Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2101262
[CH3:1][Si:2]([CH3:12])([CH3:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.Cl.[F:14][C:15]([F:27])([F:26])[O:16][C:17]1[CH:18]=[C:19]([CH2:23][CH2:24][NH2:25])[CH:20]=[CH:21][CH:22]=1.C(N(CC)CC)C.[BH4-].[Na+]>CO.O>[F:14][C:15]([F:26])([F:27])[O:16][C:17]1[CH:18]=[C:19]([CH2:23][CH2:24][NH:25][CH2:7][C:6]2[CH:9]=[CH:10][C:3]([Si:2]([CH3:12])([CH3:11])[CH3:1])=[CH:4][CH:5]=2)[CH:20]=[CH:21][CH:22]=1

Komponenten

7

Versuchsvorschrift

4-Trimethylsilanyl-benzaldehyde (178 mg, 1 mmol), 2-(3-trifluoromethoxy-phenyl)-ethyl-amine hydrochloride (241 mg, 1.1 mmol) and triethyl amine (151 mg, 1.5 mmol) were dissolved in methanol (5 ml) and the solution was stirred at rt for 5 min. Sodium borohydride (37 mg, 1 mmol) was added under nitrogen and the reaction mixture was stirred at rt for 1 h. Water was added and methanol was evaporated in vacuo. The reaction was extracted twice with diethyl ether and the combined organic layers were washed once with water and once with sat. aq. NaCl solution, dried with sodium sulfate, filtered off and concentrated in vacuo to yield [2-(3-trifluoromethoxy-phenyl)-ethyl]-(4-trimethylsilanyl-benzyl)-amine (370 mg, 100%) as a colorless oil. MS (ISP) 368.2 (100) (M+H)+.

Aufarbeitung

  1. stirringthe reaction mixture was stirred at rt for 1 h
  2. custommethanol was evaporated in vacuo
  3. extractionThe reaction was extracted twice with diethyl ether
  4. washthe combined organic layers were washed once with water and once with sat. aq. NaCl solution
  5. dry with materialdried with sodium sulfate
  6. filtrationfiltered off
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-9fce47b64154467ebe06bb2fd9e7f25d
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07572823B2

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