تفاعل #53622

ord-699c1a67994c440bbb3a41c1ddf30073

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred for 2 h
  2. 2
    workup.ADDITIONIce was added to the reaction mixtures, which
  3. 3
    استخلاصwas extracted with chloroform
  4. 4
    غسيلThe extracts were washed with brine
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    تركيزconcentrated under reduced pressure
  7. 7
    أخرىThe residue obtained
  8. 8
    أخرىwas chromatographed on aluminum oxide in ethyl acetate:hexane (1:5)

الإجراء التجريبي

LDA was prepared by addition of n-BuLi (1.56 mol/l hexane solution) 1.08 ml to a solution of diisopropylamine 255 μl in dry tetrahydrofuran 3 ml at −70° C. Then, a solution of compound (20-1) 500 mg in dry tetrahydrofuran 2 ml was added at that temperature to the mixture, which was stirred for 2 h. Then, a solution of iodine 426 mg in dry tetrahydrofuran 2 ml was added and the mixture was stirred for 2 h. Ice was added to the reaction mixtures, which was extracted with chloroform. The extracts were washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue obtained was chromatographed on aluminum oxide in ethyl acetate:hexane (1:5) to give the titled compound as colorless crystals 514 mg. Yield 76%. This was recrystallized from from acetone-isopropyl ether to give colorless crystals, m.p. 136-137° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06858640B2uspto-grants-2005_02