Réaction #1168421

Équation de réaction

HCl

N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

n-butyllithium

bromine

→

title compound

Rendement 58.7%

2-Bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

Rendement 58.7%

Solvants

diethyl ether

—

hexanes

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   Températureto warm to room temperature
3. 3
   workup.STIRRINGstir for ca. 2 hours
4. 4
   workup.STIRRINGstirred at room temperature
5. 5
   TempératureThe reaction mixture was cooled to 0° C.
6. 6
   AutreThe ether phase was separated
7. 7
   Lavagewashed with brine
8. 8
   Séchagedried (MgSO4)
9. 9
   Concentrationconcentrated in vacuo
10. 10
    AutreThe crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes)

Mode opératoire

To a solution of 8.85 g (41 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 200 ml, diethyl ether under a nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -65° C., 36.0 mL (85 mmol) 2.41M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 15 minutes. To the reaction mixture was added 2.2 ml, (41 mmol) of bromine dropwise. The light orange reaction mixture was allowed to warm to room temperature and stir for ca. 2 hours. The reaction mixture darkened as it stirred at room temperature. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The ether phase was separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes) affording 7.11 g of the title compound as an orange oil.

Source