Propanal → N,N-Bis(2-methylpropyl)prop-1-en-1-amine
Reaction equation
[CH:1](=O)[CH2:2][CH3:3].[CH2:5]([NH:9][CH2:10][CH:11]([CH3:13])[CH3:12])[CH:6]([CH3:8])[CH3:7]>>[CH2:5]([N:9]([CH:1]=[CH:2][CH3:3])[CH2:10][CH:11]([CH3:13])[CH3:12])[CH:6]([CH3:8])[CH3:7]Participants
3
Procedure
Following a procedure similar to that described in Example 64(i), but using propionaldehyde and diisobutylamine as starting materials, the title compound was obtained as a colorless oily substance (yield 29%), boiling at 63-66° C./10 mmHg
Sources & evidence
- ORD record
- ord-8072b5351fc5453583bb366260c3af1f
- Source dataset
- uspto-grants-1999_06
- Patent number
- US05908858
Reaction notes
Loading…