Sodium Iodide → HCID 54189192, compound

HRID 264908Notes

Reaction equation

HRID 264908 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[CH:8][C:9]2[O:14][CH2:13][CH:12](O)[O:11][C:10]=2[CH:16]=1)=[O:5])[CH3:2].[C:17](=[O:20])([O-])[O-].[Cs+].[Cs+].C(Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[I-].[Na+]>CC(C)=O>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]([O:20][CH2:17][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:9]2[O:14][CH2:13][CH2:12][O:11][C:10]=2[CH:16]=1)=[O:5])[CH3:2]

Participants

6

Procedure

The reaction mixture containing 900 ml of acetone, 17.4 g of hydroxy-1,4-benzodioxane-7-carboxylic acid ethyl ester, 37.9 g of caesium carbonate, 11 ml of benzyl bromide and 7.7 g of sodium iodide is stirred under reflux for 3 hours and then concentrated by evaporation. The residue is partitioned between diethyl ether and water. The organic phases are dried over sodium sulfate and concentrated by evaporation. The title compound is obtained from the residue by FC (900 g of silica gel, hexane/ethyl acetate=1:1): Rf (hexane/ethyl acetate=2:1)=0.36.

Workup

  1. temperatureunder reflux for 3 hours
  2. concentrationconcentrated by evaporation
  3. customThe residue is partitioned between diethyl ether and water
  4. dry with materialThe organic phases are dried over sodium sulfate
  5. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-8eafcfa6fb624897a4df422063567a2b
Source dataset
uspto-grants-1997_07
Patent number
US05646143

Reaction notes

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