Sodium Iodide → HCID 12235558, compound

HRID 1613321Notes

Reaction equation

HRID 1613321 reaction equation
C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[OH:9][C:10]1[CH:22]=[CH:21][C:13](/[CH:14]=[CH:15]/[C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:12][CH:11]=1.[CH2:23](Br)[CH:24]([CH3:26])[CH3:25]>CS(C)=O.O>[CH2:23]([O:9][C:10]1[CH:11]=[CH:12][C:13](/[CH:14]=[CH:15]/[C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:21][CH:22]=1)[CH:24]([CH3:26])[CH3:25]

Participants

7

Conditions

Temperature
60 °C

Procedure

13.8 g of potassium carbonate and 7.50 g of sodium iodide were added to a solution of 9.61 g of ethyl (E)-p-hydroxycinnamate and 8.22 g of isobutylbromide in 100 ml of dimethyl sulfoxide. The reaction mixture was then stirred for 20 hours at 60° C., after which it was cooled to the room temperature. The reaction mixture was then poured into 1 liter of water and extracted twice with ethyl acetate. The combined extracts were washed with water and dried over anhydrous sodium sulfate; the solvent was then removed by evaporation under reduced pressure. The residue was purified by flash column chromatography using 300 g of silica gel, eluted with a 5:1 by volume solution of hexane and ethyl acetate, to give 10.71 g of the title compound as a colorless oil (which solidified at low temperature).

Workup

  1. temperatureafter which it was cooled to the room temperature
  2. extractionextracted twice with ethyl acetate
  3. washThe combined extracts were washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was then removed by evaporation under reduced pressure
  6. customThe residue was purified by flash column chromatography
  7. washeluted with a 5:1 by volume solution of hexane and ethyl acetate

Sources & evidence

ORD record
ord-c01d6cdd2a3545c2acce05d0131ea47b
Source dataset
uspto-grants-1993_03
Patent number
US05192766

Reaction notes

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