Sodium Lauryl Sulfate → HCID 19102376, compound
Reaction equation
[C:1](#[N:3])[CH3:2].[CH3:4][NH+:5]([CH3:7])[CH3:6].[S:8]([O-:24])([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])(=[O:10])=[O:9].[Na+]>CO>[S:8]([O-:24])([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])(=[O:9])=[O:10].[C:1](#[N:3])[CH3:2].[CH3:4][NH+:5]([CH3:7])[CH3:6]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Trimethylammonium acetonitrile (1.0 g, 0.007435 mole) and sodium dodecyl sulphate (2.14 g, 0.007435 mole) were weighed into a 250 ml rotary evaporator flask. Methanol (100 ml) was added and the mixture heated until a clear solution was obtained. The methanol was evaporated off and IPA (150 ml) was added, and the mixture warmed. A granular precipitate of sodium chloride separated out and was filtered off. The amount obtained was less than the theoretical amount. The IPA-soluble fraction was evaporated to dryness to give 3.4 g of solid and this was further dried under vacuum. 'H NMR (σ, D2O) 0.9 (t, 3H, CH3 --C), 1.3 (m, 18H, CH3 (CH9) 1.7 (m, 2H, CH2CH2SO4 -), 3.4 (s, 9H, (CH3)3N+), 4.1 ppm (t, 2H, --CH2SO4-) ppm. The ratio of quaternary to dodecyl sulphate was 1.03:1.
Workup
- temperaturethe mixture heated until a clear solution
- customwas obtained
- customThe methanol was evaporated off
- additionIPA (150 ml) was added
- temperaturethe mixture warmed
- customA granular precipitate of sodium chloride separated out
- filtrationwas filtered off
- customThe amount obtained
- customThe IPA-soluble fraction was evaporated to dryness
Sources & evidence
- ORD record
- ord-4a02240ae3f74b009a04b19be771bab1
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05281361
Reaction notes
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