تفاعل #578786

ord-28a019f4643e4d9d9af8d63730c19b3c

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise, over 90 min
  2. 2
    تركيزThe reaction was concentrated to dryness
  3. 3
    workup.ADDITIONThe crude residue was treated with
  4. 4
    workup.ADDITIONa small mix of Et2O and hexanes
  5. 5
    أخرىsonicated so as
  6. 6
    أخرىto triturate out bulk of impurities, which
  7. 7
    ترشيحwere filtered off
  8. 8
    تركيزThe filtrate was concentrated to dryness
  9. 9
    أخرىThe resulting residue was purified by silica gel column chromatography
  10. 10
    غسيلto elute the title compound

الإجراء التجريبي

To a solution of 2-chloro-5-nitrophenol (3.39 g, 19.52 mmol), tetrahydrofurfuryl alcohol (1.99 g, 19.52 mmol), and Ph3P (5.12 g, 19.52 mmol) in 34 ml THF, cooled to −15° C., was added dropwise, over 90 min, a solution of DIAD (4.15 g, 20.5 mmol). The reaction was warmed to RT and stirred for 18 h. The reaction was concentrated to dryness. The crude residue was treated with a small mix of Et2O and hexanes and sonicated so as to triturate out bulk of impurities, which were filtered off. The filtrate was concentrated to dryness. The resulting residue was purified by silica gel column chromatography using EtOAc in hexanes to elute the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07531553B2uspto-grants-2009_05