Réaction #56242

ord-6a1bcab99e7646dca3cfbb7012c89a4b

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with benzene
  2. 2
    ExtractionThe benzene extract
  3. 3
    workup.STIRRINGwas shaken with 2 N aqueous sodium hydroxide
  4. 4
    Extractionextracted with ethyl acetate
  5. 5
    ExtractionThe ethyl acetate extract
  6. 6
    Lavagewas washed with water
  7. 7
    Séchagedried over anhydrous sodium sulfate
  8. 8
    Autreevaporated to dryness

Mode opératoire

To a mixture of 9-formyl-9,10-dihydro-9,10-methanoanthracene (110 mg) and β-carboxyethyltriphenylphosphonium chloride (186 mg) in dimethylsulfoxide (2 ml) and tetrahydrofuran (2 ml) was added 65.4% sodium hydride dispersion in mineral oil (37 mg) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 6 hours, diluted with water, acidified with hydrochloric acid and extracted with benzene. The benzene extract was shaken with 2 N aqueous sodium hydroxide. The basic layer was acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give γ-(9,10-dihydro-9,10-methano-9-anthryl)-β-butenoic acid. M.P. 166°-167° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04224344uspto-grants-1980_09