Butylamine → HCID 67745852, compound

HRID 465674Notes

Reaction equation

HRID 465674 reaction equation
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2C=O.[CH2:10]([NH2:14])[CH2:11][CH2:12][CH3:13].[H-].[CH2:16]([Al+]CC(C)C)C(C)C>CCCCCC>[CH:1]12[CH2:7][CH:4]([CH:3]=[CH:2]1)[CH2:5][CH2:6]2.[CH3:16][CH:11]([CH2:12][CH3:13])[CH2:10][NH2:14]

Participants

5

Conditions

Temperature
-18 °C

Procedure

79.0 g of 5-norbornene-2-carboxaldehyde (NBCXA), (77.6 ml., 0.647 mole) were dissolved in 500 ml. of hexane. 47.3 g of n-butylamine (64 ml. 0.647 mole) was slowly added at 25° C. The solution was stirred for five minutes and cooled to -18° C. for several hours. The liquid hexane layer was decanted under nitrogen to remove the precipitated water which had frozen to ice and adhered to the sides of the reaction vessel. The clean hexane solution was removed under nitrogen to a separate reactor and dried with 50 gms of dried 4A molecular sieve. After thirty minutes, the hexane layer containing the n-butyl imine of NBCXA was separated from the molecular sieves and to it was added at -10° C. 80 3 gm. (0.647 mole) of diisobutylaluminum hydride as stirred under nitrogen for one hour to yield the MFGM of 5-norbornene-2-methyl-(N-n-butyl) amine. The reactions are summarized below: ##STR39##

Workup

  1. customThe liquid hexane layer was decanted under nitrogen
  2. customto remove the precipitated water which
  3. temperaturehad frozen to ice
  4. customThe clean hexane solution was removed under nitrogen to a separate reactor
  5. customdried with 50 gms
  6. dry with materialof dried 4A molecular sieve
  7. waitAfter thirty minutes
  8. additionthe hexane layer containing the n-butyl imine of NBCXA
  9. customwas separated from the molecular sieves and to it
  10. additionwas added at -10° C

Sources & evidence

ORD record
ord-2d2c0209cc3a4f11b619879418deb832
Source dataset
uspto-grants-1992_10
Patent number
US05153282

Reaction notes

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