Sodium Iodide → 4-Iodo-2-propylphenol

HRID 2050967Notes

Reaction equation

HRID 2050967 reaction equation
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH2:2][CH3:3].[I-:11].[Na+].C(#N)C.C(OCl)(C)(C)C>C(OCC)(=O)C.O>[I:11][C:8]1[CH:7]=[CH:6][C:5]([OH:10])=[C:4]([CH2:1][CH2:2][CH3:3])[CH:9]=1

Participants

7

Procedure

A mixture of 6.8 g (50 mmol) of 2-propylphenol. 8.25 g (55 mmol) of sodium iodide. 175 ml of acetonitrile and 40 ml of water was cooled on ice. t-Butylhypochlorite, 6 g or 6.56 ml (55 mmol), was added slowly at 0° . After stirring for 10 minutes at 0° , 500 ml of ethyl acetate was added and the mixture was washed with 5% aqueous solution of sodium thiosulfate. The organic layer was dried and evaporated and the residue was chromatographed over 150 g of silica gel using methylene chloride/hexane 3:2. The more polar monoiodinated product was crystallized from petroleum ether to give colorless crystals with m.p. 54°-56°.

Workup

  1. washthe mixture was washed with 5% aqueous solution of sodium thiosulfate
  2. customThe organic layer was dried
  3. customevaporated
  4. customthe residue was chromatographed over 150 g of silica gel
  5. customThe more polar monoiodinated product was crystallized from petroleum ether
  6. customto give colorless crystals with m.p. 54°-56°

Sources & evidence

ORD record
ord-38b7fa4c82194d5091b383ca55d7867b
Source dataset
uspto-grants-1991_05
Patent number
US05015661

Reaction notes

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