تفاعل #1135092

ord-5516e07943a64b788dabf210adde8d75

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONA stirring bar is added
  2. 2
    workup.ADDITIONis added
  3. 3
    أخرىis completely consumed
  4. 4
    workup.ADDITIONby slowly adding dilute aqueous HCl (3%, ˜6 mL)
  5. 5
    workup.ADDITIONThe contents of the flask are poured into a separatory funnel which
  6. 6
    أخرىThe layers are separated
  7. 7
    استخلاصThe aqueous layer is extracted with EtOAc (20 mL)
  8. 8
    غسيلThe combined organic extracts are washed with water (20 mL) and brine (20 mL)
  9. 9
    تجفيفdried over MgSO4
  10. 10
    ترشيحfiltered
  11. 11
    تركيزconcentrated

الإجراء التجريبي

A 100 mL flask containing 2-[(2,2-difluoro-1,3-benzodioxole-4-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (0.38 g, 0.98 mmol) is charged with 1,4-dioxane (6 mL) and MeOH (6 mL). A stirring bar is added and stirring is initiated. After dissolution, water (3 mL) is added followed by the LiOH monohydrate (103 mg, 2.46 mmol). After 70 h, tlc analysis (silica, 10% MeOH/DCM) indicates that the starting material is completely consumed. The pH of the reaction mixture is carefully adjusted to pH 2 by slowly adding dilute aqueous HCl (3%, ˜6 mL). The contents of the flask are poured into a separatory funnel which contains EtOAc (30 mL). The layers are separated. The aqueous layer is extracted with EtOAc (20 mL). The combined organic extracts are washed with water (20 mL) and brine (20 mL), dried over MgSO4, filtered and concentrated by pumping to constant weight to give off white solid (0.33 g, 94%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08569535B2uspto-grants-2013_10