Réaction #1224
ord-2f9353d568ba495d9d6fa8a66d2c0875
Équation de réaction
4-iodo-2-trichloroacetylpyrrole
methanol
sodium methoxide
→
methyl 4-iodo-2-pyrrolecarboxylate
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autrethe reaction medium evaporated to dryness
- 2Autrethe residue obtained
- 3AutreThe organic phase was decanted off
- 4Séchagedried over magnesium sulfate
- 5Autreevaporated
- 6AutreThe residue obtained
- 7Autrewas triturated in heptane
- 8Filtrationfiltered
- 9Autre4.9 g (81%) of the expected ester of melting point 77°-78° C. were recovered
Mode opératoire
8.2 g (24 mmol) of 4-iodo-2-trichloroacetylpyrrole and 100 ml of methanol were introduced into a round-bottomed flask and 2 g (36 mmol) of sodium methoxide were added. The mixture was stirred at room temperature for four hours, the reaction medium evaporated to dryness, and the residue obtained taken up in water and ethyl ether. The organic phase was decanted off, dried over magnesium sulfate and evaporated. The residue obtained was triturated in heptane and filtered; 4.9 g (81%) of the expected ester of melting point 77°-78° C. were recovered.