Pyridine → 3-Amino-4-iodo-benzophenone

HRID 1017792Notes

Reaction equation

HRID 1017792 reaction equation
[I:1][C:2]1[CH:15]=[CH:14][C:5]([C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:7])=[CH:4][C:3]=1[N+:16]([O-])=O.S(S([O-])=O)([O-])=O.[Na+].[Na+].N1C=CC=CC=1>O>[NH2:16][C:3]1[CH:4]=[C:5]([CH:14]=[CH:15][C:2]=1[I:1])[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7]

Participants

5

Conditions

Temperature
40 °C

Procedure

A mixture of 5.0 g (14 mmol) of 4-iodo-3-nitro-benzophenone, 7.5 g (42 mmol) of sodium dithionite, 40 ml of pyridine and 15 ml of water is heated to 40° C. for 2 hours. Then the mixture is concentrated in vacuo, combined with ice water and extracted with ethyl acetate. The organic phase is dried with sodium sulphate and the solvent is distilled off in vacuo.

Workup

  1. concentrationThen the mixture is concentrated in vacuo
  2. extractionextracted with ethyl acetate
  3. dry with materialThe organic phase is dried with sodium sulphate
  4. distillationthe solvent is distilled off in vacuo

Sources & evidence

ORD record
ord-3b9cd23a6a8f4bd8aaf0982c10cd3699
Source dataset
uspto-grants-2002_11
Patent number
US06479524B1

Reaction notes

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