Réaction #2446059
ord-21343fccb3b947d39218c09389aad346
Équation de réaction
4-picoline
acetonitrile
1-bromo-2-[(2-bromoethyl)disulphanyl]ethane
N-methylpyrrolidone
→
expected product
Rendement 90.0%
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(4-methylpyridinium)dibromide
Rendement 90.0%
Réactifs
Aucun
Conditions de réaction
Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.ADDITIONis added over 5 minutes
- 2Températurethe mixture is cooled
- 3AutreThe solid obtained
- 4Filtrationis filtered off
- 5Lavagerinsed with 3×200 ml of acetonitrile
- 6workup.DISSOLUTIONdissolved in 800 ml of isopropanol (at reflux)
- 7TempératureAfter cooling
- 8workup.ADDITION1 l of ethyl ether is added
- 9AutreThe precipitate formed
- 10Filtrationis filtered off
- 11Lavagerinsed with 3×200 ml of ethyl ether
- 12Autredried
- 13AutreThe 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.