반응 #63554

ord-4d3ab34c7ec543f8a4e739c64817eae9

반응 방정식

O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[K+]
potassium iodide
Oc1ccc(Oc2ccccc2)cc1
4-phenoxyphenol
CCOC(CBr)OCC
bromoacetaldehyde diethyl acetal
CCOC(COc1ccc(Oc2ccccc2)cc1)OCC
4-phenoxyphenoxyacetaldehyde diethyl acetal

반응 조건

온도
150°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The salts are then removed by filtration from the reaction solution
  2. 2
    workup.DISTILLATIONmost of the dimethylformamide is distilled off in a water jet vacuum
  3. 3
    workup.DISSOLUTIONThe residue is dissolved in ether
  4. 4
    세척the resultant solution is washed twice with water, three times with 20% potassium hydroxide solution and again with water
  5. 5
    건조The ethereal solution is then dried over sodium sulfate
  6. 6
    workup.DISTILLATIONthe ether is distilled off entirely
  7. 7
    기타The resultant 4-phenoxyphenoxyacetaldehyde diethyl acetal is used without further purification for the preparation of the free aldehyde

실험 절차

150 g of potassium carbonate and 4 g of finely powdered potassium iodide are added to a solution of 112 g (0.6 mole) of 4-phenoxyphenol and 157.6 g (0.8 mole) of bromoacetaldehyde diethyl acetal in 480 ml of dimethylformamide, and the batch is heated, under nitrogen, for 14 hours at 150° C. The salts are then removed by filtration from the reaction solution, and most of the dimethylformamide is distilled off in a water jet vacuum. The residue is dissolved in ether and the resultant solution is washed twice with water, three times with 20% potassium hydroxide solution and again with water. The ethereal solution is then dried over sodium sulfate and the ether is distilled off entirely. The resultant 4-phenoxyphenoxyacetaldehyde diethyl acetal is used without further purification for the preparation of the free aldehyde.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04766152uspto-grants-1988_08