Sodium Hydroxide → HCID 47382, Verbindung

HRID 1395025Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1395025
[CH:1](=[N:3][C:4]([CH2:11][CH2:12][CH3:13])([CH2:8][CH2:9][CH3:10])[CH2:5][CH2:6][CH3:7])[CH3:2].[BH4-].[Na+].[OH-].[Na+]>CO>[CH2:1]([NH:3][C:4]([CH2:11][CH2:12][CH3:13])([CH2:5][CH2:6][CH3:7])[CH2:8][CH2:9][CH3:10])[CH3:2]

Komponenten

5

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Into a 500-ml three-necked flask, fitted with a mechanical stirrer and a condenser, were introduced 17.6 g (0.096 mol) of N-ethylidene-1,1-di-n-propyl-n-butylamine, prepared as described hereabove, and 150 ml of methanol. To this solution when cooled, 7.6 g (0.2 mol) of sodium borohydride were added slowly and while stirring. After this operation, the mixture was maintained at a temperature of 5° C. for 30 minutes and then progressively heated under reflux. Thirty minutes later, the methanol was evaporated off under vacuum and 200 ml of water were added to the residue so obtained followed by 100 ml of a solution of sodium hydroxide (d=1.38). The organic fraction was extracted with ether and the solution was distilled under reduced pressure.

Aufarbeitung

  1. customInto a 500-ml three-necked flask, fitted with a mechanical stirrer and a condenser
  2. customprepared
  3. temperatureTo this solution when cooled
  4. temperatureprogressively heated
  5. temperatureunder reflux
  6. customThirty minutes later, the methanol was evaporated off under vacuum and 200 ml of water
  7. additionwere added to the residue
  8. customso obtained
  9. extractionThe organic fraction was extracted with ether
  10. distillationthe solution was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9b2c2316baee449fbc592e555d7e5e93
Quelldatensatz
uspto-grants-1980_05
Patentnummer
US04201725

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