Potassium Iodide → HCID 20334282, compound

HRID 1706715Notes

Reaction equation

HRID 1706715 reaction equation
[OH:1][C:2]1[C:11]([CH3:12])=[C:10]2[C:5]([C:6](=[O:15])[CH2:7][C:8]([CH3:14])([CH3:13])[O:9]2)=[CH:4][CH:3]=1.[CH2:16](Cl)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-:25].[K+].[K+].[I-].[K+]>CC(C)=O>[C:16]([O:1][C:2]1[C:11]([CH3:12])=[C:10]2[C:5]([C:6](=[O:15])[CH2:7][C:8]([CH3:13])([CH3:14])[O:9]2)=[CH:4][CH:3]=1)(=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

6

Procedure

The mixture of 10.3 g. of the compound obtained in (1), 8.2 g. of benzyl chloride, 10.2 g. of potassium carbonate, 0.5 g. of potassium iodide, and 100 ml of acetone was refluxed for 2 hours. The mixture was then filtered, and the filtrate was concentrated. Ether was added to the concentrate. The ether layer was washed successively with water, 1 N aqueous sodium hydroxide, and again with water. The solution was dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane, to obtain 12.2 g. (yield: 82.4%) of the subject compound.

Workup

  1. additionThe mixture of 10.3 g
  2. filtrationThe mixture was then filtered
  3. concentrationthe filtrate was concentrated
  4. additionEther was added to the concentrate
  5. washThe ether layer was washed successively with water, 1 N aqueous sodium hydroxide
  6. dry with materialThe solution was dried over magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe residue was recrystallized from ethyl acetate/n-hexane
  9. customto obtain 12.2 g

Sources & evidence

ORD record
ord-d6c4c24cf436424cb038d0ab6a3520ad
Source dataset
uspto-grants-1980_06
Patent number
US04208426

Reaction notes

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