Isophorone diisocyanate → Ipdi jeffamine
Reaction equation
[CH3:1][CH:2]([NH2:17])[CH2:3][O:4][CH2:5][CH:6]([O:8][CH2:9][CH:10]([O:12][CH2:13][CH:14]([NH2:16])[CH3:15])[CH3:11])[CH3:7].[O:18]=[C:19]=[N:20][CH:21]1[CH2:30][C:29]([CH3:32])([CH3:31])[CH2:28][C:23]([CH3:33])([CH2:24][N:25]=[C:26]=[O:27])[CH2:22]1>CC(O)C>[CH3:31][C:29]1([CH3:32])[CH2:28][C:23]([CH2:24][N:25]=[C:26]=[O:27])([CH3:33])[CH2:22][CH:21]([N:20]=[C:19]=[O:18])[CH2:30]1.[CH3:1][CH:2]([NH2:17])[CH2:3][O:4][CH2:5][CH:6]([O:8][CH2:9][CH:10]([O:12][CH2:13][CH:14]([NH2:16])[CH3:15])[CH3:11])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of JEFFAMINE® D-400 (160 g, 0.40 m) and i-PrOH (120) was charged into a flask. Isophorone diisocyanate (44.4 g, 0.20) was added dropwise at 20°-25° C. over a 1 hour period of time. The solvent in the product solution was removed by using a high vacuum. The resulting product was a colorless semisolid at room temperature. The analysis of amine indicated 1.59 meq/g.
Workup
- additionwas charged into a flask
- customThe solvent in the product solution was removed
- customat room temperature
Sources & evidence
- ORD record
- ord-6f0676e649ce4275bccaebaf8bba2280
- Source dataset
- uspto-grants-1991_04
- Patent number
- US05010160
Reaction notes
Loading…