反应 #2346366

反应方程式

HCl

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

n-butyllithium

N,N-dimethylformamide

→

title compound

收率 39.0%

N-(1,1-Dimethylethyl)-2-formyl-1-methyl-1H-pyrrole-3-sulfonamide

收率 39.0%

溶剂

THF

—

hexanes

反应条件

后处理

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   温度to warm to room temperature
3. 3
   workup.STIRRINGstir for ca. 2 hours
4. 4
   温度The reaction mixture was cooled to 0° C.
5. 5
   其他The THF phase was separated
6. 6
   洗涤washed with brine
7. 7
   干燥dried (MgSO4)
8. 8
   浓缩concentrated in vacuo
9. 9
   其他The crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes)

实验过程

To a solution of 12.96 g (60 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 300 mL THF under a nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -65° C., 52.35 mL (123 mmol) 2.35M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added 4.64 mL (60 mmol) of N,N-dimethylformamide dropwise. The reaction mixture was allowed to warm to room temperature and stir for ca. 2 hours. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF 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 5.72 g of the title compound as a white solid, m.p. 101.5°-103° C. 1H NMR (CDCl3, 200 MHz.) δ: 10.25(s,1H), 6.81(d,1H), 6.6(d,1H), 4.93(bs,1H), 3.98(s,3H), 1.27(s,9H).

来源