Reaktion #1221

ord-5222a695140643c8a668e63555fad359

Reaktionsgleichung

CC1(C)CCC(C)(C)c2cc3cc(Br)ccc3cc21
5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-bromoanthracene
[Mg]
magnesium
CCOC(=O)c1csc(Br)c1
ethyl 2-bromo-4-thiophenecarboxylate
CCOC(=O)c1csc(-c2ccc3cc4c(cc3c2)C(C)(C)CCC4(C)C)c1
ethyl 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-4-thiophenecarboxylate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONOnce the addition
  2. 2
    Temperaturthe mixture was heated
  3. 3
    Temperaturat reflux for one hour
  4. 4
    Temperaturthe mixture was maintained
  5. 5
    workup.STIRRINGunder stirring at room temperature for 12 hours
  6. 6
    workup.ADDITIONThe reaction medium was poured into ice-cold water
  7. 7
    Extraktionextracted with ethyl ether
  8. 8
    Sonstigethe organic phase decanted off
  9. 9
    Trocknendried over magnesium sulfate
  10. 10
    Sonstigeevaporated
  11. 11
    SonstigeThe residue obtained
  12. 12
    Sonstigewas chromatographed on a silica column
  13. 13
    Wascheneluted with a mixture of hexane and dichloromethane (60/40)
  14. 14
    SonstigeAfter evaporation of the solvents, 6.35 g (74%) of the expected ester of melting point 107°-108° C.
  15. 15
    Sonstigewere recovered

Vorschrift

A solution of 9.5 g (30 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-bromoanthracene was added dropwise to a suspension of 724 mg (30 mmol) of magnesium in 10 ml of THF. Once the addition was completed, the mixture was heated at reflux for one hour. At room temperature 4.1 g (30 mmol) of anhydrous zinc chloride were added and the mixture was stirred for one hour. 5.2 g (22 mmol) of ethyl 2-bromo-4-thiophenecarboxylate and 120 mg (0.22 mmol) of the complex NiCl2 /DPPE were then added successively and the mixture was maintained under stirring at room temperature for 12 hours. The reaction medium was poured into ice-cold water, extracted with ethyl ether, the organic phase decanted off, dried over magnesium sulfate and evaporated. The residue obtained was chromatographed on a silica column eluted with a mixture of hexane and dichloromethane (60/40). After evaporation of the solvents, 6.35 g (74%) of the expected ester of melting point 107°-108° C. were recovered.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723499uspto-grants-1998_03