Reaction #2446059
ord-21343fccb3b947d39218c09389aad346
Reaction equation
4-picoline
acetonitrile
1-bromo-2-[(2-bromoethyl)disulphanyl]ethane
N-methylpyrrolidone
→
expected product
Yield 90.0%
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(4-methylpyridinium)dibromide
Yield 90.0%
Reagents
None
Conditions
Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1workup.ADDITIONis added over 5 minutes
- 2Temperaturethe mixture is cooled
- 3OtherThe solid obtained
- 4Filtrationis filtered off
- 5Washrinsed with 3×200 ml of acetonitrile
- 6workup.DISSOLUTIONdissolved in 800 ml of isopropanol (at reflux)
- 7TemperatureAfter cooling
- 8workup.ADDITION1 l of ethyl ether is added
- 9OtherThe precipitate formed
- 10Filtrationis filtered off
- 11Washrinsed with 3×200 ml of ethyl ether
- 12Otherdried
- 13OtherThe off-white powder obtained (73.77 g)
Procedure
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.