Acetonitrile → 1,1'-(Disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide

HRID 655085

Reaktionsgleichung

Reaktionsgleichung von HRID 655085
[Br:1][CH2:2][CH2:3][S:4][S:5][CH2:6][CH2:7]Br.[CH3:9][N:10]1[CH2:14][CH2:13][CH2:12][C:11]1=O.[N:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22].[C:23](#N)C>>[Br-:1].[Br-:1].[S:5]([CH2:6][CH2:7][N+:10]1[CH:9]=[CH:14][CH:13]=[CH:12][C:11]=1[CH3:23])[S:4][CH2:3][CH2:2][N+:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22]

Komponenten

5

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 56 g of 1-bromo-2-[(2-bromoethyl)-disulphanyl]ethane and 15 ml of N-methylpyrrolidone (NMP) is poured dropwise onto 35 g of 2-picoline with stirring, at 80° C. The mixture (white suspension) is kept stirring at 80° C. for 30 min, 100 ml of acetonitrile (ACN) are added, and the stirring is maintained at 80° C. for 90 min. After cooling, the solid obtained is filtered off, washed with 100 ml of ACN and then dried. 56.2 g of brown powder are recovered. 45 g of this powder are suspended in 300 ml of isopropanol (iPrOH), at reflux. Once the temperature has dropped to 40° C., the solid is filtered off, washed with 3 times 100 ml of iPrOH and dried under vacuum. 40.56 g of a light beige product are obtained. The analyses are in conformity with the expected structure.

Aufarbeitung

  1. stirringThe mixture (white suspension) is kept stirring at 80° C. for 30 min
  2. temperaturethe stirring is maintained at 80° C. for 90 min
  3. temperatureAfter cooling
  4. customthe solid obtained
  5. filtrationis filtered off
  6. washwashed with 100 ml of ACN
  7. customdried
  8. custom56.2 g of brown powder are recovered
  9. temperatureat reflux
  10. additionOnce the temperature has dropped to 40° C.
  11. filtrationthe solid is filtered off
  12. washwashed with 3 times 100 ml of iPrOH
  13. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-2a140e2d7035494484d0accf27d4cc9a
Quelldatensatz
uspto-grants-2011_12
Patentnummer
US08070830B2

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