Sodium Iodide → HCID 20320776, compound

HRID 866392Notes

Reaction equation

HRID 866392 reaction equation
Cl/[CH:2]=[CH:3]/[C:4]([CH:6]1[CH2:9][C:8]2([CH2:12][CH2:11][CH2:10]2)[CH2:7]1)=[O:5].[I-:13].[Na+]>CC(C)=O>[I:13]/[CH:2]=[CH:3]/[C:4]([CH:6]1[CH2:9][C:8]2([CH2:12][CH2:11][CH2:10]2)[CH2:7]1)=[O:5]

Participants

4

Procedure

1-Chloro-3-(spiro[3.3]hept-2-yl)-1E-propen-3-one (7.3 g, 0.042 mole) was mixed with 25.2 g (0.168 mole) of sodium iodide and 45 ml of dry acetone (distilled from anhydrous potassium carbonate, b.p. 56° C). The mixture was refluxed with rapid stirring overnight. The mixture was cooled and the solvent was removed in vacuo. The solid residue was taken up in 75 ml of water and the products were extracted with 150 ml (3×50 ml) of ether. The organic material was washed with 50 ml of saturated sodium bicarbonate solution, 50 ml of aqueous sodium thiosulfate solution and 50 ml of saturated sodium chloride solution. The material was dried over anhydrous magnesium sulfate, filtered and the solvent was removed in vacuo to yield 6.9 g (62.2%) of crude 1-iodo-3-(spiro[3.3]hept-2-yl)-1E-propen-3-one.

Workup

  1. temperatureThe mixture was refluxed
  2. temperatureThe mixture was cooled
  3. customthe solvent was removed in vacuo
  4. extractionthe products were extracted with 150 ml (3×50 ml) of ether
  5. washThe organic material was washed with 50 ml of saturated sodium bicarbonate solution, 50 ml of aqueous sodium thiosulfate solution and 50 ml of saturated sodium chloride solution
  6. dry with materialThe material was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-f0b7d444b87a476792deff1346e53b79
Source dataset
uspto-grants-1978_07
Patent number
US04098823

Reaction notes

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