تفاعل #48096

ord-ad2ed7ffac5a46c2b080c82832390b4b

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThen, the solution is concentrated under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue is dissolved in THF (100 mL)
  3. 3
    درجة الحرارةThe resulting solution is cooled in an ice-bath
  4. 4
    workup.ADDITIONLiBH4 (3.4 g) is added in portions
  5. 5
    أخرىThe cooling bath is removed
  6. 6
    workup.STIRRINGthe mixture is stirred at room temperature for 1 h
  7. 7
    workup.ADDITIONThe reaction mixture is diluted with THF
  8. 8
    workup.ADDITIONtreated with 0.1 M hydrochloric acid
  9. 9
    أخرىThen, the organic layer is separated
  10. 10
    استخلاصthe aqueous layer is extracted with ethyl acetate
  11. 11
    تجفيفThe combined organic layers are dried (Na2SO4)
  12. 12
    أخرىthe solvent is evaporated under reduced pressure

الإجراء التجريبي

Oxalyl chloride (13.0 mL) is added to an ice-cold solution of 2-bromo-5-iodo-benzoic acid in CH2Cl2 (200 mL). DMF (0.2 mL) is added and the solution is stirred at room temperature for 6 h. Then, the solution is concentrated under reduced pressure and the residue is dissolved in THF (100 mL). The resulting solution is cooled in an ice-bath and LiBH4 (3.4 g) is added in portions. The cooling bath is removed and the mixture is stirred at room temperature for 1 h. The reaction mixture is diluted with THF and treated with 0.1 M hydrochloric acid. Then, the organic layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic layers are dried (Na2SO4) and the solvent is evaporated under reduced pressure to give the crude product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745414B2uspto-grants-2010_06