反应 #2314346

ord-6c25de1ddb0e4ccda6f8d6df6ca1d695

反应方程式

Cc1cccc(N)n1
2-amino-6-picoline
[O-][I+3]([O-])([O-])O
periodic acid
II
iodine
O=S(=O)(O)O
sulfuric acid
O=S([O-])O.[Na+]
sodium bisulfite
Cc1nc(N)ccc1I
2-amino-5-iodo-6-picoline
收率 161.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取The aqueous solution is extracted with diethyl ether (3×100 mL)
  2. 2
    洗涤The combined organics are washed with 10% NaOH
  3. 3
    干燥dried over Na2SO4
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated
  6. 6
    其他Purification by chromatography (eluent EtOAc)
  7. 7
    其他affords a yellow liquid
  8. 8
    其他The liquid is further dried on the vacuum pump where it
  9. 9
    其他crystallizes

实验过程

A mixture of 2-amino-6-picoline (5.40 g), periodic acid (2.28 g), and iodine (5.00 g) is heated in a solution of acetic acid (30 mL), water (6 mL), and sulfuric acid (0.9 mL) at 80° C. for 3 h. The reaction is cooled to room temperature and poured into 100 mL 10% aqueous sodium bisulfite. The aqueous solution is extracted with diethyl ether (3×100 mL). The combined organics are washed with 10% NaOH, then dried over Na2SO4, filtered, and concentrated. Purification by chromatography (eluent EtOAc) affords a yellow liquid. The liquid is further dried on the vacuum pump where it crystallizes to afford 2-amino-5-iodo-6-picoline (4.48 g, 38%). Physical characteristics are as follows: 1H NMR (300 MHz, DMSO-d6) δ 7.60, 6.09, 6.05, 2.38.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06413958B2uspto-grants-2002_07