تفاعل #339229
ord-dc8fbf935eeb49aea0a563ef7043f5a5
معادلة التفاعل
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1تركيزconcentrated
- 2أخرىto remove acetone
- 3workup.ADDITIONThe residual aqueous solution was diluted with NaHCO3
- 4استخلاصextracted with 2×EtOAc
- 5تجفيفThe combined organic layer was dried over Na2SO4
- 6ترشيحfiltered
- 7تركيزconcentrated
- 8أخرىThe 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%).