反应 #1435775

ord-53a20fc3df5941e8ba2bc65252e79304

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONAfter complete addition
  2. 2
    workup.STIRRINGstirring
  3. 3
    workup.WAITcontinued at 0° C. for 3 hours
  4. 4
    其他at room temperature
  5. 5
    其他overnight
  6. 6
    其他the solvent was evaporated under reduced pressure
  7. 7
    workup.ADDITIONthe residue treated with 100 ml of hydrochloric acid (1 N)
  8. 8
    萃取extracted 3 times with 150 ml of ethyl acetate
  9. 9
    其他The crude product (4.0 g) was obtained as a dark brown oil which
  10. 10
    其他was purified by flash-chromatography on silica gel using a gradient of a 100%
  11. 11
    workup.ADDITION0%- to 50%:50%-mixture of heptane and ethyl acetate as the eluent

实验过程

In an inert atmosphere and under exclusion of moisture, at 0° C. a solution of 1.5 g (10 mmol) of 2-methyl-6-nitro-phenol [Ger.Offen. 3536192] in 30 ml of N,N-dimethylformamide was treated portionwise with 0.42 g (18 mmol) of sodium hydride (55% dispersion in mineral oil). After complete addition, stirring was continued for 1 hour at 0° C. Thereafter, 3.85 g (11 mmol) of (S)-2,2-dioxo-2λ6-[1,2,3]oxathiazolidine-3,4-dicarboxylic acid 4-benzyl ester 3-tert-butyl ester was added and stirring continued at 0° C. for 3 hours, then at room temperature overnight. For the working-up, the solvent was evaporated under reduced pressure, the residue treated with 100 ml of hydrochloric acid (1 N), then extracted 3 times with 150 ml of ethyl acetate. The crude product (4.0 g) was obtained as a dark brown oil which was purified by flash-chromatography on silica gel using a gradient of a 100%:0%- to 50%:50%-mixture of heptane and ethyl acetate as the eluent. There were obtained 1.4 g (33%) of the title compound as an yellow oil, [α]589=−1.45° (c=1.0% in MeOH), MS m/e (%): 431.4 (M+H+, 13).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211573B2uspto-grants-2007_05