تفاعل #339229

ord-dc8fbf935eeb49aea0a563ef7043f5a5

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated
  2. 2
    أخرىto remove acetone
  3. 3
    workup.ADDITIONThe residual aqueous solution was diluted with NaHCO3
  4. 4
    استخلاصextracted with 2×EtOAc
  5. 5
    تجفيفThe combined organic layer was dried over Na2SO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe crude product was purified by chromatography (20% to 50% EtOAc/hexanes)

الإجراء التجريبي

A solution of (3,3-dimethyl-1,5-dioxa-spiro[5,5]undec-9-yl)-methyl-carbamic acid tert-butyl ester (9.53 g, 27.2 mmol, 1.0 eq.) and PPTS (2.1 g, 0.3 eq.) in acetone-water (2:1, 500 mL) was heated at 80° C. for 18 h, cooled to room temperature and concentrated to remove acetone. The residual aqueous solution was diluted with NaHCO3 and extracted with 2×EtOAc. The combined organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by chromatography (20% to 50% EtOAc/hexanes) to give methyl-(4-oxo-cyclohexyl)-carbamic acid tert-butyl ester as a white solid (5.38 g, 87%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07868002B2uspto-grants-2011_01