反应 #742267

ord-2a140e2d7035494484d0accf27d4cc9a

反应方程式

CC#N
acetonitrile
BrCCSSCCBr
1-bromo-2-[(2-bromoethyl)-disulphanyl]ethane
CN1CCCC1=O
N-methylpyrrolidone
Cc1ccccn1
2-picoline
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
light beige product
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
1,1′-(disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGThe mixture (white suspension) is kept stirring at 80° C. for 30 min
  2. 2
    温度the stirring is maintained at 80° C. for 90 min
  3. 3
    温度After cooling
  4. 4
    其他the solid obtained
  5. 5
    过滤is filtered off
  6. 6
    洗涤washed with 100 ml of ACN
  7. 7
    其他dried
  8. 8
    其他56.2 g of brown powder are recovered
  9. 9
    温度at reflux
  10. 10
    workup.ADDITIONOnce the temperature has dropped to 40° C.
  11. 11
    过滤the solid is filtered off
  12. 12
    洗涤washed with 3 times 100 ml of iPrOH
  13. 13
    其他dried under vacuum

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08070830B2uspto-grants-2011_12