تفاعل #595515

ord-cc082869a817405284e5dfc444244742

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىIn a 2 L, 3-neck round-bottom flask equipped with an overhead stirrer
  2. 2
    أخرىto give an orange solution
  3. 3
    غسيلwashed with 1M aqueous HCl (3×250 mL)
  4. 4
    غسيلThe dichloromethane layer was then washed sequentially with saturated aqueous NaHCO3, water, and saturated aqueous NaCl
  5. 5
    تجفيفThe dichloromethane layer was dried over sodium sulfate
  6. 6
    workup.ADDITIONtreated simultaneously with decolorizing charcoal for 30 min
  7. 7
    ترشيحthe solution then filtered through Celite
  8. 8
    تركيزthe filtrate was concentrated
  9. 9
    workup.DISSOLUTIONThe pink/orange solid was dissolved in a minimal amount of hot ethyl acetate (50-75 mL)
  10. 10
    workup.ADDITIONslowly diluted with hexanes (500-600 ml)
  11. 11
    أخرىto give orange crystals that
  12. 12
    ترشيحwere collected by filtration
  13. 13
    أخرىdried

الإجراء التجريبي

In a 2 L, 3-neck round-bottom flask equipped with an overhead stirrer was added 4-ethynylaniline (30 g, 256 mmol) and pyridine (42.5 ml, 525 mmol) in dichloromethane (512 ml) to give an orange solution. The mixture was cooled to 5° C. and methanesulfonyl chloride (19.96 ml, 256 mmol) was added drop wise over 15 min. The reaction solution was stirred at 5° C. for 2 h and washed with 1M aqueous HCl (3×250 mL). The dichloromethane layer was then washed sequentially with saturated aqueous NaHCO3, water, and saturated aqueous NaCl. The dichloromethane layer was dried over sodium sulfate and treated simultaneously with decolorizing charcoal for 30 min, the solution then filtered through Celite and the filtrate was concentrated. The pink/orange solid was dissolved in a minimal amount of hot ethyl acetate (50-75 mL) and slowly diluted with hexanes (500-600 ml) to give orange crystals that were collected by filtration and dried to provide the title compound (40.0 g, 80%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095590B2uspto-grants-2015_08