Sulfuric Acid → 3-Iodo-4-cyclohexylphenylglyoxylic acid

HRID 839405

Reaktionsgleichung

Reaktionsgleichung von HRID 839405
N[C:2]1[CH:3]=[C:4]([C:14](=[O:20])[C:15]([O:17]CC)=[O:16])[CH:5]=[CH:6][C:7]=1[CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:30].[K+]>[Cu].O>[I:30][C:2]1[CH:3]=[C:4]([C:14](=[O:20])[C:15]([OH:17])=[O:16])[CH:5]=[CH:6][C:7]=1[CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To 0.05 moles of ethyl 3-amino-4-cyclohexylphenylglyoxylate dissolved in a mixture of 50 g. of ice water and .06 moles of concentrated sulfuric acid at 0° C is added a solution of 0.05 moles of 95% sodium nitrite in 8 ml. of water. Stirring is continued for 1/2 hour and then 1.5 ml. of concentrated sulfuric acid is added. This solution is poured into an ice cold solution of 0.06 moles of potassium iodide in 10 ml. of water. To this is added 0.075 g. copper bronze with stirring and the solution is warmed slowly on a water bath to about 80° C for 2 hours. After cooling to room temperature the reaction mixture is extracted thrice with 15 ml. portions of chloroform. This is then washed with dilute thiosulfate solution, water, dried over sodium sulfate and evaporated in vacuo. The residue is crystallized to obtain 3-iodo-4-cyclohexylphenylglyoxylic acid.

Aufarbeitung

  1. additionTo this is added 0.075 g
  2. temperatureAfter cooling to room temperature the reaction mixture
  3. extractionis extracted thrice with 15 ml
  4. washThis is then washed with dilute thiosulfate solution, water
  5. dry with materialdried over sodium sulfate
  6. customevaporated in vacuo
  7. customThe residue is crystallized

Quellen und Nachweise

ORD-Eintrag
ord-73960826bd3a444ebcfb95129ca78a0a
Quelldatensatz
uspto-grants-1978_06
Patentnummer
US04094995

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