Réaction #2446059

ord-21343fccb3b947d39218c09389aad346

Équation de réaction

Cc1ccncc1
4-picoline
CC#N
acetonitrile
BrCCSSCCBr
1-bromo-2-[(2-bromoethyl)disulphanyl]ethane
CN1CCCC1=O
N-methylpyrrolidone
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
expected product
Rendement 90.0%
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(4-methylpyridinium)dibromide
Rendement 90.0%

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONis added over 5 minutes
  2. 2
    Températurethe mixture is cooled
  3. 3
    AutreThe solid obtained
  4. 4
    Filtrationis filtered off
  5. 5
    Lavagerinsed with 3×200 ml of acetonitrile
  6. 6
    workup.DISSOLUTIONdissolved in 800 ml of isopropanol (at reflux)
  7. 7
    TempératureAfter cooling
  8. 8
    workup.ADDITION1 l of ethyl ether is added
  9. 9
    AutreThe precipitate formed
  10. 10
    Filtrationis filtered off
  11. 11
    Lavagerinsed with 3×200 ml of ethyl ether
  12. 12
    Autredried
  13. 13
    AutreThe off-white powder obtained (73.77 g)

Mode opératoire

67 g of 4-picoline are diluted in 100 ml of acetonitrile and the mixture is heated to 80° C. A mixture of 60 g of 1-bromo-2-[(2-bromoethyl)disulphanyl]ethane and 15 ml of N-methylpyrrolidone (NMP) is added over 5 minutes. After 4 hours of stirring at 85° C., the mixture is cooled. The solid obtained is filtered off, rinsed with 3×200 ml of acetonitrile and then dissolved in 800 ml of isopropanol (at reflux). After cooling, 1 l of ethyl ether is added. The precipitate formed is filtered off, rinsed with 3×200 ml of ethyl ether and then dried. The off-white powder obtained (73.77 g) contains a great majority (>90%) of the expected product, which is used as it is for the following step.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08685114B2uspto-grants-2014_04