Peracetic Acid → HCID 20314474, compound

HRID 2419911Notes

Reaction equation

HRID 2419911 reaction equation
[C:1]([O:4]O)(=[O:3])[CH3:2].[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[CH:18]=[CH:17][C:16]([I:19])=[CH:15][CH:14]=2)=[CH:9][CH:8]=1>C(O)(=O)C>[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]2[CH:18]=[CH:17][C:16]([I:19]([O:4][C:1]([CH3:2])=[O:3])[O:4][C:1]([CH3:2])=[O:3])=[CH:15][CH:14]=2)=[CH:11][CH:12]=1

Participants

4

Reactant 2

HCID 6585Peracetic AcidHCID 43042304-Chloro-4'-iodobiphenyl

Product 1

HCID 20314474HCID 20314474, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
30 °C

Procedure

Peracetic acid (40%, 13 ml.) is added dropwise to a stirred suspension of 4-(4-chlorophenyl)iodobenzene (12.6 g.) in acetic acid (25 ml.) at 30° C. during 1 hour. The mixture is stirred at 30° C. for 6 hours, and at ambient temperature for 2 days, then evaporated to dryness in vacuo. The residue is washed with light petroleum, and is crystallised from chloroform to give 4-(4-chlorophenyl)-(diacetoxyliodo)benzene (10.7 g.) m.p. 147°-150° C.

Workup

  1. waitat ambient temperature for 2 days
  2. customevaporated to dryness in vacuo
  3. washThe residue is washed with light petroleum
  4. customis crystallised from chloroform

Sources & evidence

ORD record
ord-94f2016bfdb641e1bf2e6fc4cee059e6
Source dataset
uspto-grants-1978_08
Patent number
US04107329

Reaction notes

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