Reacción #95387
ord-f770c4c3d4424493bd96bf077e2c6ba2
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaheating the reaction mixture sufficiently
- 2workup.DISTILLATIONto distill off the water that
- 3Otrois formed as
- 4Otroa result of the reaction
- 5Otroat room temperature
- 6workup.WAITwill be completed in a relatively short period of time, with only an hour
- 7Otrotwo 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).