Benzaldehyde → HCID 18920515, compound
Reaction equation
[CH2:1]([CH2:7][CH2:8][CH2:9][NH2:10])[CH2:2][CH2:3][CH2:4][CH2:5][NH2:6].[CH:11](=O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[H][H]>C(O)C>[C:12]1([CH2:11][N:6]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][CH2:7][CH2:8][CH2:9][NH2:10])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Combine 14.4 gm of diaminooctane, 20.3 ml of benzaldehyde and 0.66 gm of Pt2O in 100 ml of ethanol. Treat the resulting mixture with hydrogen at 45 lbs./sq.in. until no further hydrogen is taken up. Filter, evaporate the solvent (in vacuo), and distill the rendered material to obtain 25.5 gm of the desired product, bp 185°-190° C. at 0.1 mm.
Workup
- filtrationFilter
- customevaporate the solvent (in vacuo)
- distillationdistill the rendered material
Sources & evidence
- ORD record
- ord-7e22f8c55c9b4c27b1ca41dccd3b98b5
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05753714
Reaction notes
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