Sodium Laurate → Trimethylammonium acetonitrile laurate

HRID 1198375

Reaktionsgleichung

Reaktionsgleichung von HRID 1198375
[Cl-].[C:2](#[N:4])[CH3:3].[CH3:5][NH+:6]([CH3:8])[CH3:7].[C:9]([O-:22])(=[O:21])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].[Na+].C([O-])(=O)CCCCCCCCCCC>CO>[C:9]([O-:22])(=[O:21])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].[C:2](#[N:4])[CH3:3].[CH3:5][NH+:6]([CH3:8])[CH3:7]

Komponenten

5

Versuchsvorschrift

Trimethylammonium acetonitrile chloride (1.0 g, 0.007435 mole) was dissolved in methanol (20 ml) in a test tube. Sodium laurate (1.65 g, 0.007435 mole) was dissolved in boiling methanol (50 ml) and the two solutions mixed. The solution was evaporated to dryness and the solid heated with ethanol (60 ml). A granular precipitate of sodium chloride settled out and was filtered off, but less than the theorectical amount was obtained. The ethanolic solution was evaporated to dryness, azeotroped twice with IPA to give a lumpy solid containing white and fawn components (2.08 g, yield 93%). 'H NMR (σ, D2O) 0.85 (t, 3H, CH3-) 1.3 (s, I6H, CH3 -(CH2)8), 1.55 (m, 2H, CH2CH2CO-) 3.4 (s, 9H, (CH3)3N+) ppm. The ratio of quat to laurate was 1.3:1.

Aufarbeitung

  1. additionthe two solutions mixed
  2. customThe solution was evaporated to dryness
  3. temperaturethe solid heated with ethanol (60 ml)
  4. filtrationwas filtered off
  5. customless than the theorectical amount was obtained
  6. customThe ethanolic solution was evaporated to dryness
  7. customazeotroped twice with IPA
  8. customto give a lumpy solid
  9. additioncontaining white

Quellen und Nachweise

ORD-Eintrag
ord-dbc5b480494c4541a91a422562b60c2b
Quelldatensatz
uspto-grants-1994_01
Patentnummer
US05281361

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