Bis(2-ethylhexyl)amine → HCID 19826647, compound
Reaction equation
[CH:1]1([N:7]=[C:8]=[N:9][CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:16][CH2:17][CH2:18][CH2:19][CH:20]([CH2:23][NH:24][CH2:25][CH:26]([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:27][CH3:28])[CH2:21][CH3:22]>C(O)(C)(C)C>[CH2:27]([CH:26]([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:25][N:24]([CH2:23][CH:20]([CH2:21][CH3:22])[CH2:19][CH2:18][CH2:17][CH3:16])[C:8]([NH:7][CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1)=[N:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)[CH3:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
41.3 Gm. (0.2 mole) of dicyclohexylcarbodiimide, 72.4 gm. (0.3 mole) of bis-2-ethylhexylamine, and 200 ml. of t-butanol were refluxed for 7 hours. The t-butanol was distilled off at atmospheric pressure and the residue stripped to a temperature of 180° C. at 0.08-0.09 mm Hg. The residue weighed 60.8 gm. and was 90% pure by NMR with a trace of amine and approximately 5% dicyclohexylcarbodiimide.
Workup
- distillationThe t-butanol was distilled off at atmospheric pressure
- customstripped to a temperature of 180° C. at 0.08-0.09 mm Hg
Sources & evidence
- ORD record
- ord-f6b809a823464d2db4ecd9f60b9401cf
- Source dataset
- uspto-grants-1991_07
- Patent number
- US05028259
Reaction notes
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