反应 #2200611

ord-3b63b07ad6dc4b52b454a0d2f1ab8457

反应方程式

CCCCn1ccnc1
1-butylimidazole
Cc1cc(C)c(S(=O)(=O)ON)c(C)c1
O-mesitylene sulfonylhydroxylamine
CCOCC
ether
CCCC[n+]1ccn(N)c1.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
1-butyl-3-aminoimidazolium mesitylene sulfonate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.WAITto stand at −16° C. overnight
  3. 3
    过滤The product was recovered by filtration
  4. 4
    洗涤washed with a mixture of CH2Cl2: ether (3:1 v/v)
  5. 5
    其他to yield a white amorphous powder
  6. 6
    其他The crude product was recrystallized from a mixture of CH2Cl2 (80 mL) and ether (80 mL)
  7. 7
    其他to give 12.40 g

实验过程

An ice-cold solution of 1-butylimidazole (7.0 g, 16.30 mmol) in anhydrous CH2Cl2 (35 mL) was treated dropwise with a solution of O-mesitylene sulfonylhydroxylamine (17.8 g, 16.50 mmol) in CH2Cl2 (70 mL). After stirring for 6 hours in the ice-bath, ether (210 mL) was added with stirring over the course of 1 hour. The resulting mixture was allowed to stand at −16° C. overnight. The product was recovered by filtration, and washed with a mixture of CH2Cl2: ether (3:1 v/v) to yield a white amorphous powder; 16.70 g. The crude product was recrystallized from a mixture of CH2Cl2 (80 mL) and ether (80 mL) to give 12.40 g; mp 71-73° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07432254B2uspto-grants-2008_10