تفاعل #2446059

ord-21343fccb3b947d39218c09389aad346

معادلة التفاعل

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
المردود 90.0%
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(4-methylpyridinium)dibromide
المردود 90.0%

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685114B2uspto-grants-2014_04