Reacción #95387

ord-f770c4c3d4424493bd96bf077e2c6ba2

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheating the reaction mixture sufficiently
  2. 2
    workup.DISTILLATIONto distill off the water that
  3. 3
    Otrois formed as
  4. 4
    Otroa result of the reaction
  5. 5
    Otroat room temperature
  6. 6
    workup.WAITwill be completed in a relatively short period of time, with only an hour
  7. 7
    Otrotwo at the most being required for the reaction

Procedimiento

Once the 1-(2-hydroxyethyl)pyrrole is obtained, it is esterified by any suitable means known in the art. Suitably, acetic acid is reacted with the 1-(2-hydroxyethyl)pyrrole in the presence of a strong acid such as sulfuric acid and heating the reaction mixture sufficiently to distill off the water that is formed as a result of the reaction. Preferably however, the pyrrole is reacted with acetyl chloride or acetic anhydride in a suitable solvent wherein there is a molar excess of the acetyl chloride or acetic anhydride. The reaction takes place at room temperature and will be completed in a relatively short period of time, with only an hour or two at the most being required for the reaction to reach completion. The 1-(2-acetoxyethyl)pyrrole is then isolated and purified by any means known in the art such as extraction with a suitable organic solvent and removal of the solvent to yield the desired compound represented by Formula (III).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04344943uspto-grants-1982_08