反应 #1244266

ord-94f3dca8ca374516a351a0e6caa52d4b

反应方程式

Cc1ccc(S(=O)(=O)OCC(O)CN=[N+]=[N-])cc1
3-Azido-2-hydroxypropyl 4-methylbenzenesulfonate
CC(=O)OC(C)=O
acetic anhydride
CC(=O)OC(CN=[N+]=[N-])COS(=O)(=O)c1ccc(C)cc1
15
收率 98.8%
CC(=O)OC(CN=[N+]=[N-])COS(=O)(=O)c1ccc(C)cc1
1-Azido-3-(tosyloxy)propan-2-yl acetate
收率 98.8%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at room temperature
  2. 2
    workup.ADDITIONsilica was added to the reaction mixture
  3. 3
    其他the solvent was evaporated
  4. 4
    其他the residue was purified on silica gel using 50% EtOAc/hexanes as the eluent

实验过程

3-Azido-2-hydroxypropyl 4-methylbenzenesulfonate 14 (1.83 g, 6.70 mmol) was dissolved in CH2Cl2 (15 mL) and treated with TEA (1.4 mL, 10.00 mmol), a catalytic amount of DMAP and acetic anhydride (0.95 mL, 10.00 mmol) at room temperature. After stirring for 1 hr, silica was added to the reaction mixture, the solvent was evaporated and the residue was purified on silica gel using 50% EtOAc/hexanes as the eluent to afford 2.07 g of 15 (98.8% yield) as a thick, clear, colorless oil. 1H NMR (CDCl3, 400 MHz) δ: 7.79 (d, J=8.4 Hz, 2H), 7.37 (d, J=8.0 Hz, 2H), 5.02-5.07 (m, 1H), 4.09-4.21 (m, 2H), 3.43-3.53 (m, 2H), 2.46 (s, 3H), 2.05 (s, 3H). Mass Spec (lo-res): Calc'd for C12H15N3O5S: 313.07. found: 314.1 (M+H+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07807394B2uspto-grants-2010_10