Isopropanol → HCID 86619918, Verbindung

HRID 495260Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 495260
CC(O)C.[CH2:5]([P:9]([CH2:12][CH:13]([CH3:15])[CH3:14])(=[S:11])[SH:10])[CH:6]([CH3:8])[CH3:7].[OH-].[CH2:17]([N+:21]([CH2:30][CH2:31][CH2:32][CH3:33])([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:22][CH2:23][CH2:24][CH3:25])[CH2:18][CH2:19][CH3:20].CCCCCC>O>[CH2:5]([P:9]([CH2:12][CH:13]([CH3:15])[CH3:14])(=[S:10])[S-:11])[CH:6]([CH3:8])[CH3:7].[CH2:30]([N+:21]([CH2:17][CH2:18][CH2:19][CH3:20])([CH2:22][CH2:23][CH2:24][CH3:25])[CH2:26][CH2:27][CH2:28][CH3:29])[CH2:31][CH2:32][CH3:33]

Komponenten

6

Versuchsvorschrift

To 40 ml of 2-propanol, 3.63 g diisobutyldithiophosphinic acid and 7.34 g of 55-60% by weight tetrabutylammonium hydroxide in water were added. The mixture was stirred under nitrogen for one hour. The solvent was removed by distillation. To remove residual water, 2-propanol was twice added and subsequently removed by distillation. The liquid was cooled to less than OC for 16 hours. To the precipitates that formed, a small amount of hexane was added to give a slurry. The slurry was filtered, washed with hexane, and dried under reduced pressure yielding 6.07 g of a white solid.

Aufarbeitung

  1. customThe solvent was removed by distillation
  2. customTo remove residual water, 2-propanol
  3. additionwas twice added
  4. customsubsequently removed by distillation
  5. temperatureThe liquid was cooled to less than OC for 16 hours
  6. customTo the precipitates
  7. customthat formed
  8. customto give a slurry
  9. filtrationThe slurry was filtered
  10. washwashed with hexane
  11. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b1b62a77c53f4a40a62cd0491ba3644d
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07538931B2

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