Lauryldimethylamine → HCID 129726115, compound
Reaction equation
[CH2:1]([CH:3]1[O:5][CH2:4]1)[Br:2].[CH2:6]([N:18]([CH3:20])[CH3:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]>O1CCOCC1>[Br-:2].[CH2:6]([N+:18]([CH3:20])([CH3:19])[CH2:1][CH:3]1[O:5][CH2:4]1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
In a reaction flask was placed 12.4 grams of epibromohydrin, 18.73 grams of dodecyldimethyl amine and 21.34 grams of para-dioxane solvent. This was stirred and heated under nitrogen to reflux (ca. 90° C.). After 6 hours at reflux the mixture was cooled. Solvent removed under vacuum to afford product, dodecyl dimethyl (2,3-epoxypropyl) ammonium bromide as a clear gel.
Workup
- customIn a reaction flask was placed
- temperatureheated under nitrogen
- temperatureAfter 6 hours at reflux the mixture
- temperaturewas cooled
- customSolvent removed under vacuum
Sources & evidence
- ORD record
- ord-6e822c1dc55a484bbf8cedf1ca5efa72
- Source dataset
- uspto-grants-1989_11
- Patent number
- US04883917
Reaction notes
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