Adipic Acid → HCID 86747076, compound
Reaction equation
[OH:1][CH2:2][C:3]([CH2:8][OH:9])([CH2:6][OH:7])[CH2:4][OH:5].[C:10]([OH:29])(=[O:28])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27].[C:30]([OH:39])(=[O:38])[CH2:31][CH2:32][CH2:33][CH2:34][C:35]([OH:37])=[O:36].[CH2:40]([C:42]([CH2:47][OH:48])([CH3:46])[C:43]([OH:45])=[O:44])[OH:41].[Sn]>>[CH2:40]([C:42]([CH2:47][OH:48])([CH3:46])[C:43]([OH:45])=[O:44])[OH:41].[C:10]([OH:29])(=[O:28])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27].[C:30]([OH:39])(=[O:38])[CH2:31][CH2:32][CH2:33][CH2:34][C:35]([OH:37])=[O:36].[OH:1][CH2:2][C:3]([CH2:8][OH:9])([CH2:6][OH:7])[CH2:4][OH:5]Participants
6
Procedure
As in Example N, 76.2 g (0.56 mole) pentaerythritol, 302.4 g (1.12 mole) technical stearic acid, 71.5 g (0.49 mole) adipic acid and 9.4 g (0.07 mole) dimethylolpropionic acid instead of tartaric acid were reacted in three steps using a total of 1.0 g tin powder. After the addition of bleaching earth, filtration under pressure at 90° C. and cooling, the pentaerythritol adipate stearate dimethylolpropionate (8:7:16:1) (material Q; 364 g) was present as a yellowish, brittle wax-like mass (dropping point 52.8° C.; acid number 2.7; saponification number 289.0; hydroxyl number 28.0).
Workup
- additionAfter the addition
- filtrationearth, filtration under pressure at 90° C.
- temperaturecooling
- custombrittle wax-like mass (dropping point 52.8° C.; acid number 2.7; saponification number 289.0; hydroxyl number 28.0)
Sources & evidence
- ORD record
- ord-d0c2f871bafc43ff91b9f755f4fc3668
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05232967
Reaction notes
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