Tetraethylammonium Hydroxide → HCID 86760339, compound
Reaction equation
[C:1]([OH:24])(=[O:23])[CH2:2][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][CH2:20][CH2:21][CH3:22].[OH-].[CH2:26]([N+:28]([CH2:33][CH3:34])([CH2:31][CH3:32])[CH2:29][CH3:30])[CH3:27]>O>[C:1]([O-:24])(=[O:23])[CH2:2][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][CH2:20][CH2:21][CH3:22].[CH2:26]([N+:28]([CH2:33][CH3:34])([CH2:31][CH3:32])[CH2:29][CH3:30])[CH3:27]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
A mixture of 100 g water, 8.95 g of behenic acid (20 mmole), and 8.0 g of a 35 weight % solution of tetraethylammonium hydroxide was heated to 70° C. with stirring. Then an additional 0.16 g of the tetraethylammonium hydroxide solution was added to adjust the pH to 8.3 (˜20 mmole total). The resulting opalescent solution was freeze dried to yield a white free-flowing powder.
Workup
- customdried
- customto yield a white free-flowing powder
Sources & evidence
- ORD record
- ord-2132300be16c4c88ae9828826e80f518
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07153635B1
Reaction notes
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