Sodium Lauryl Sulfate → HCID 19102376, compound

HRID 1198376Notes

Reaction equation

HRID 1198376 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

4

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

  1. temperaturethe mixture heated until a clear solution
  2. customwas obtained
  3. customThe methanol was evaporated off
  4. additionIPA (150 ml) was added
  5. temperaturethe mixture warmed
  6. customA granular precipitate of sodium chloride separated out
  7. filtrationwas filtered off
  8. customThe amount obtained
  9. 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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