Dipropylamine → HCID 86629339, compound
Reaction equation
[C:1]([O-:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([NH:9][CH2:10][CH2:11][CH3:12])[CH2:7][CH3:8].C(C1C=CC(P([O-])([O-])[O-])=C(CCCCCCCCC)C=1CCCCCCCCC)CCCCCCCC>>[C:1]([O-:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([NH:9][CH2:10][CH2:11][CH3:12])[CH2:7][CH3:8]Participants
4
Procedure
To 200 g of the acrylate obtained in Example 1.A, 10.7 g of dipropylamine was added in order to reach in the end product, a nitrogen content of 0.75%. After the slight exotherm observed during addition of the amine, the reaction mixture was maintain at 50° C. until the free dipropylamine content reached 1000 ppm, as measured by titration. After being stripped to reach a free dipropylamine content below 200 ppm, the end product was post-stabilized with 5000 ppm trisnonylphenylphosphite. A clear, low odour, low viscous (viscosity C/P (25° C.)=185 mPa·s) and low colored (0.6 Gardner) product was obtained.
Workup
- customA clear, low odour, low viscous (viscosity C/P (25° C.)=185 mPa·s) and low colored (0.6 Gardner) product was obtained
Sources & evidence
- ORD record
- ord-c77f70612ef0425cb0548b76fee66e74
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266987B2
Reaction notes
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