반응 #1168416

반응 방정식

Methyl chloroformate

HCl

n-butyllithium

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

→

title compound

Methyl 3-[[(1,1-dimethylethyl)amino]sulfonyl]-1-methyl-1H-pyrrole-2-carboxylate

용매

—

hexanes

THF

반응 조건

후처리

1. 1
   workup.ADDITIONwas added dropwise at such a rate as
2. 2
   기타the temperature below -65° C
3. 3
   온도to warm to room temperature
4. 4
   workup.STIRRINGstirred for ca. 1.5 hours
5. 5
   온도was cooled to 0° C.
6. 6
   기타The THF phase was separated
7. 7
   세척washed with brine
8. 8
   건조dried (MgSO4)
9. 9
   농축concentrated to an amber oil
10. 10
    기타The NMR of the crude reaction product

실험 절차

To a solution of 1 g (4.62 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 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. 4.1 mL (9.48 mmol) 2.32M n-butyllithium in hexanes. The resulting amber turbid solution was stirred at -78° C. for ca. 30 minutes. Methyl chloroformate (0.37 mL, 4.86 mmol) was added in one portion and the resulting gold reaction mixture was allowed to warm to room temperature and stirred for ca. 1.5 hours. The gold reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated washed with brine, dried (MgSO4) and concentrated to an amber oil. The NMR of the crude reaction product was consistent with the title compound, additionally the NMR indicated that a trace of the starting material was also present. The crude material was combined with the product from a similar reaction run on the scale described below and chromatographed to give the title compound.

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