Ammonia → Eicosenyl succinimide
Reaction equation
[CH:1]([CH:21]1[CH2:26][C:25](=[O:27])O[C:22]1=[O:23])=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].[NH3:28]>>[CH:1]([CH:21]1[CH2:26][C:25](=[O:27])[NH:28][C:22]1=[O:23])=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]Participants
3
Conditions
- Temperature
- 160 °C
Procedure
In another reaction vessel was placed 570 grams of the above isomerized eicosenyl succinic anhydride. This was heated to 160° C. and ammonia injection started. The temperature rose to 175° C. Ammonia injection was continued at 175° C. until the temperature dropped. Then 30" Hg vacuum was slowly applied to distill out water and ammonia. Additional ammonia was injected to be sure no anhydride remained. There was no further reaction so this ammonia was stripped out at 30" Hg vacuum at 170° C. yielding isomerized eicosenyl succinimide.
Workup
- customIn another reaction vessel was placed
- customrose to 175° C
- customwas continued at 175° C. until the temperature
- additiondropped
- distillationto distill out water and ammonia
- customno further reaction so this ammonia
- customwas stripped out at 30" Hg vacuum at 170° C.
Sources & evidence
- ORD record
- ord-abfdafdc498447db847686bb5a73f369
- Source dataset
- uspto-grants-1986_09
- Patent number
- US04613341
Reaction notes
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