Réaction #915
ord-952e75b6acac43568991fc07fe11133a
Équation de réaction
2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
TFA
→
title compound
Rendement 21.4%
2-Bromo-1-methyl-1H-pyrrole-3-sulfonamide
Rendement 21.4%
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1ConcentrationThe reaction mixture was concentrated in vacuo
- 2workup.ADDITIONThree portions of diethyl ether were added to the crude residue
- 3Autrewas removed by evaporation
- 4Autreto remove residual TFA, which
Mode opératoire
To a solution of 7.11 g (24 mmol) of 2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 50 mL methylene chloride under a nitrogen atmosphere was added 50 mL of TFA. The reaction mixture was allowed to stir at room temperature overnight ca. 16 hours. The reaction mixture was concentrated in vacuo. Three portions of diethyl ether were added to the crude residue and was removed by evaporation to remove residual TFA, which yielded 1.23 g of the title compound as a light brown solid.