Water → 1-(diphenylmethyl)-N-ethyl-3-azetidinemethanamine

HRID 622554Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 622554
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]1([CH:13]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:14]2[CH2:17][CH:16]([C:18]([NH:20][CH2:21][CH3:22])=O)[CH2:15]2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.O.[OH-].[Na+]>O1CCCC1>[C:7]1([CH:13]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:14]2[CH2:17][CH:16]([CH2:18][NH:20][CH2:21][CH3:22])[CH2:15]2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Komponenten

6

Versuchsvorschrift

To a suspension of 3.2 g (85 mmole) of lithium aluminum hydride in 50 ml of dry tetrahydrofuran was added dropwise, a solution of 8.5 g (28.0 mmole) of 1-(diphenylmethyl)-N-ethyl-3-azetidinecarboxamide in 50 ml of dry tetrahydrofuran. After the addition was complete, the reaction was refluxed for two hours, cooled to room temperature, and decomposed by the successive addition of 3.4 ml of water, 3.4 ml of 15% aqueous sodium hydroxide and 10.2 ml of water, titrating the final water addition to give a granular precipitate. The inorganic precipitate was removed by filtration, washed with tetrahydrofuran and evaporated in vacuo to give 6.7 g of 1-(diphenylmethyl)-N-ethyl-3-azetidinemethanamine as a heavy syrup. This was used without further purification.

Aufarbeitung

  1. additionwas added dropwise
  2. additionAfter the addition
  3. temperaturethe reaction was refluxed for two hours
  4. customto give a granular precipitate
  5. customThe inorganic precipitate was removed by filtration
  6. washwashed with tetrahydrofuran
  7. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-9cb13c0e1bea4fe5ac55a6540c62e520
Quelldatensatz
uspto-grants-1988_09
Patentnummer
US04771054

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