Acetic Acid → Methyl 2,4-dichloro-5-iodobenzoate

HRID 217284Notes

Reaction equation

HRID 217284 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[C:8]([I:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:13][Si](C=[N+]=[N-])(C)C.C(O)(=O)C>ClCCl.CO>[CH3:13][O:5][C:4](=[O:6])[C:3]1[CH:7]=[C:8]([I:12])[C:9]([Cl:11])=[CH:10][C:2]=1[Cl:1]

Participants

6

Procedure

Sodium iodate (4.4 g) and iodine (11.1 g) were added to 90% sulfuric acid (330 mL), and stirred at room temperature for 8 hours. 2,4-Dichlorobenzoic acid (21 g) commercially available was added and stirred at the same temperature for 24 hours. The reaction solution was poured into ice water (3 L), and the precipitated solid material was collected by filtration. Further, the solid material was washed with water, and dried under reduced pressure. 2,4-Dichloro-5-iodobenzoic acid (16.8 g) was obtained by recrystallization (acetic acid-water). The resulting 2,4-dichloro-5-iodobenzoic acid (2 g) was dissolved in a mixture of dichloromethane (20 mL) and methanol (20 mL). Trimethylsilyldiazomethane (hexane solution, 2 M) was added dropwise until the solution became yellow. A small amount of acetic acid was added, and then the resulting mixture was concentrated under reduced pressure. The resulting residue was recrystallized using hexane to give the title compound 2,4-dichloro-5-iodobenzoic acid methyl ester as white solid (2 g).

Workup

  1. concentrationthe resulting mixture was concentrated under reduced pressure
  2. customThe resulting residue was recrystallized

Sources & evidence

ORD record
ord-2136f648dc024f56b555e0c8764ac0c8
Source dataset
uspto-grants-2012_06
Patent number
US08193351B2

Reaction notes

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