Methanol → Methyl 4-Iodo-3-methylbenzoate

HRID 840487

Reaktionsgleichung

Reaktionsgleichung von HRID 840487
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[I:11])[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.[CH3:17]O>>[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[I:11])[C:5]([O:7][CH3:17])=[O:6]

Komponenten

4

Versuchsvorschrift

24.4 g (0.093 mol) of 3-methyl-4-iodobenzoic acid and 250 ml of methanol were introduced into a round-bottomed flask and 2.5 ml of concentrated sulfuric acid were added dropwise. Heating was carried out at reflux for twelve hours, the reaction mixture was evaporated and the residue taken up in ethyl acetate and water. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue was triturated in methanol and filtered. 21.9 g (85%) of the expected methyl ester, with a melting point of 58°-59° C., were recovered.

Aufarbeitung

  1. temperatureHeating
  2. temperatureat reflux for twelve hours
  3. customthe reaction mixture was evaporated
  4. customThe organic phase was separated
  5. dry with materialdried over magnesium sulfate
  6. customevaporated
  7. customThe residue was triturated in methanol
  8. filtrationfiltered
  9. custom21.9 g (85%) of the expected methyl ester, with a melting point of 58°-59° C., were recovered

Quellen und Nachweise

ORD-Eintrag
ord-28e714b4d999404bbb4c92a95d3104a7
Quelldatensatz
uspto-grants-2002_04
Patentnummer
US06368608B1

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