반응 #42732

ord-ef4ea43a78ff495cb8c3230a83042d2f

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter another 30 minutes
  2. 2
    workup.WAITAfter 10 minutes
  3. 3
    기타the reaction was quenched
  4. 4
    workup.ADDITIONby diluting the reaction mixture with diethyl ether
  5. 5
    workup.ADDITIONpouring it onto 500 mL of 5% aqueous Na2SO3
  6. 6
    workup.ADDITIONpremixed with 500 mL of 5% aqueous NaHCO3
  7. 7
    기타The phases were separated
  8. 8
    세척the organic phase was washed with brine
  9. 9
    건조dried over Na2SO4
  10. 10
    여과filtered
  11. 11
    농축concentrated under reduced pressure

실험 절차

To the product of step (b) (23.4 g, 0.113 mol) in 600 mL of THF at −78° C. was added 135 mL of 1.0 M sodium hexamethyldisilazane in THF (Sigma-Aldrich). After 1 hour, trimethylsilyl chloride (15.8 mL, 0.124 mol) was added. After another 30 minutes, bromine (5.82 mL, 0.113 mol) was added. After 10 minutes, the reaction was quenched by diluting the reaction mixture with diethyl ether and pouring it onto 500 mL of 5% aqueous Na2SO3 premixed with 500 mL of 5% aqueous NaHCO3. The phases were separated and the organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound as an oil that solidified upon storage in the freezer.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732441B2uspto-grants-2010_06