Glycolic Acid → N,N'-(1,6-hexylene)-bis[2-hydroxyundecylamine] diglycolate
Reaction equation
[CH2:1]([NH:20][CH2:21][CH:22]([OH:32])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][NH:7][CH2:8][CH:9]([OH:19])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:33]([OH:37])(=[O:36])[CH2:34][OH:35].C[OH:39]>>[C:33]([OH:37])(=[O:36])[CH2:34][O:35][CH2:23][C:22]([OH:32])=[O:39].[CH2:1]([NH:20][CH2:21][CH:22]([OH:32])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][NH:7][CH2:8][CH:9]([OH:19])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]Participants
4
Procedure
A solution of N,N'-(1,6-hexylene-bis[2-hydroxyundecylamine] (5 g.), glycolic acid (1.66 g.) and methanol was heated until the solids dissolved, then evaporated to dryness. Recrystallization of the solid from acetone afforded N,N'-(1,6-hexylene)-bis[2-hydroxyundecylamine] diglycolate (4.6 g., m.p. 88.2°-94.6° C.).
Workup
- dissolutiondissolved
- customevaporated to dryness
- customRecrystallization of the solid from acetone
Sources & evidence
- ORD record
- ord-90d35a0d60104635b37f5d246ba94c40
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119668
Reaction notes
Loading…