反应 #1094

ord-e6119d1ed5fd4cad8ff5deeb55d6be7b

反应方程式

O=CO
formic acid
CC(=O)OC(C)=O
acetic anhydride
COC(=O)c1ccc(N)cc1S(=O)(=O)NC(C)(C)C
N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide
COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture is subsequently heated at 50°-60° C. for 2 h
  2. 2
    其他The cooling bath is removed
  3. 3
    workup.STIRRINGThe reaction mixture is then shaken up in 800 ml of ethyl acetate
  4. 4
    洗涤washed with three times 150 ml of water
  5. 5
    干燥The organic phase is dried over magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent is distilled off
  7. 7
    其他the residue is recrystallized from ethyl acetate/n-heptane

实验过程

6.5 ml of formic acid are carefully added at 0° C. to 13 ml of acetic anhydride. The mixture is subsequently heated at 50°-60° C. for 2 h. A solution of 16.0 g (0.056 mol) of N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide in 50 ml of DMF is then added dropwise at 0° C. The cooling bath is removed and the mixture is stirred for a further 4 h at room temperature. The reaction mixture is then shaken up in 800 ml of ethyl acetate and washed with three times 150 ml of water. The organic phase is dried over magnesium sulfate, the solvent is distilled off, and the residue is recrystallized from ethyl acetate/n-heptane. The product is N-tert-butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide (14.23 g, 82% of theory) which melts at 113°-114° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723409uspto-grants-1998_03