Reaktion #2692

ord-20a28c547f764190864154877d314000

Reaktionsgleichung

O=C=O
carbon dioxide
CI
methyl iodide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[Li][CH2]CCC
n-Butyllithium
CC1(C)Sc2cc3c(cc2S1)SC(C)(C)S3
2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole
COC(=O)c1c2c(cc3c1SC(C)(C)S3)SC(C)(C)S2
4-Methoxycarbonyl-(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole)

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONfilled
  2. 2
    Sonstigereaction flask
  3. 3
    workup.STIRRINGafter stirring overnight
  4. 4
    Filtrationthe ether was filtered off
  5. 5
    WaschenThe solid residue was washed with chloroform
  6. 6
    Sonstigedried under vacuum
  7. 7
    workup.STIRRINGwas stirred for 1.5 h at 60° C
  8. 8
    workup.WAITThe stirring was continued overnight
  9. 9
    FiltrationThe mixture was filtered
  10. 10
    Sonstigethe solution evaporated
  11. 11
    workup.DISSOLUTIONthe residue was dissolved in dichloromethane
  12. 12
    WaschenThe organic phase was washed with water (2*30 mL)
  13. 13
    Trocknendried (Na2SO4)
  14. 14
    Sonstigeevaporated
  15. 15
    Sonstigeto give
  16. 16
    Sonstigeafter additional drying under vacuum a bright green-yellow crystalline pure product

Vorschrift

2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole (2.0 g, 6.98 mmol) was dissolved in dry ether (50.0 mL) in a dry, argon filled reaction flask. n-Butyllithium (3.07 mL, 2.5M in hexane) was added and the reaction mixture was stirred for 30 min. The solution was poured onto solid carbon dioxide and, after stirring overnight, the ether was filtered off. The solid residue was washed with chloroform and dried under vacuum. The crude product was mixed with potassium carbonate (0.97 g, 6.98 mmol) in dry DMF (20.0 mL) and was stirred for 1.5 h at 60° C. After cooling to ambient temperature, methyl iodide (0.435 mL, 6.98 mmol) was added. The stirring was continued overnight. The mixture was filtered, the solution evaporated and the residue was dissolved in dichloromethane and water. The organic phase was washed with water (2*30 mL), dried (Na2SO4) and evaporated to give after additional drying under vacuum a bright green-yellow crystalline pure product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728370uspto-grants-1998_03