反应 #1340621

ord-e54b86242a4746faa63a87612ad05887

反应方程式

II
iodine
ClCCl
CH2Cl2
O=C([O-])[O-].[Ca+2]
CaCO3
COC(=O)c1cc(I)c(N)cc1Cl
Methyl 4-amino-2-chloro-5-iodo-benzoate
COC(=O)c1cc(I)c(N)cc1Cl
70n
COC(=O)c1cc(I)c(N)cc1Cl
methyl 4-amino-2-chloro-5-iodo-benzoate
COC(=O)c1ccc(N)c(I)c1Cl
methyl 4-amino-2-chloro-3-iodo-benzoate
COC(=O)c1cc(I)c(N)cc1Cl
methyl 4-amino-2-chloro-5-iodo-benzoate

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The resulting reaction mixture
  2. 2
    浓缩The reaction mixture was concentrated
  3. 3
    其他partitioned between EtOAc and water
  4. 4
    浓缩The organic layer was concentrated
  5. 5
    其他purified by flash column chromatography (silica gel, 20-25% EtOAc/hexanes)

实验过程

Methyl 4-amino-2-chloro-5-iodo-benzoate, 70n. To a suspension of compound 70m (1.18 g, 6.38 mmol) and CaCO3 (12.8 mmol, 1.28 g) in MeOH (13 mL) was added a solution of iodine monchloride (6.70 mmol, 1.09 g) in CH2Cl2 (6 mL) dropwise at room temperature. The resulting reaction mixture was stirred at room temperature for 1.5 h. The reaction mixture was concentrated and then partitioned between EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 20-25% EtOAc/hexanes) to provide methyl 4-amino-2-chloro-5-iodo-benzoate 70n as major the product and methyl 4-amino-2-chloro-3-iodo-benzoate 70o as the minor product.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08455476B2uspto-grants-2013_06