반응 #51864

반응 방정식

water

thiophenol

N-allyl-N-{2-[3-(S)-(tert-butyl-dimethyl-silanyloxy)-pyrrolidin-1-yl]-2-oxo-1-(S)-phenyl-ethyl}-2-nitro-benzenesulfonamide

potassium carbonate

→

title compound

수율 97.1%

2-Allylamino-1-[3-(S)-(tert-butyl-dimethyl-silanyloxy)-pyrrolidin-1-yl]-2-(S)-phenyl-ethanone

수율 97.1%

용매

dimethylformamide

반응 조건

후처리

1. 1
   workup.STIRRINGThe mixture was stirred for 16 hours at ambient temperature
2. 2
   추출extracted with ethyl acetate (3×150 cm3)
3. 3
   세척The combined ethyl acetate extracts were washed with water (2×100 cm3), brine (1×100 cm3)
4. 4
   건조dried over sodium sulfate, vacuum
5. 5
   여과filtered
6. 6
   기타the volatile fractions removed in vacuo to a foul smelling yellow oil
7. 7
   기타The crude product was purified by column chromatography (silica, eluting with hexane-ethyl acetate 1:1 to 0:1)

실험 절차

To a stirred solution N-allyl-N-{2-[3-(S)-(tert-butyl-dimethyl-silanyloxy)-pyrrolidin-1-yl]-2-oxo-1-(S)-phenyl-ethyl}-2-nitro-benzenesulfonamide (8.73 g, 15.6 mmol) in anhydrous dimethylformamide (45 cm3) was added potassium carbonate (6.50 g, 46.8 mmol). The mixture was stirred at ambient temperature for 10 minutes and thiophenol (2.25 cm3, 21.8 mmol) was added dropwise over 10 minutes. The mixture was stirred for 16 hours at ambient temperature and poured into water (500 cm3) and extracted with ethyl acetate (3×150 cm3). The combined ethyl acetate extracts were washed with water (2×100 cm3), brine (1×100 cm3), dried over sodium sulfate, vacuum filtered and the volatile fractions removed in vacuo to a foul smelling yellow oil. The crude product was purified by column chromatography (silica, eluting with hexane-ethyl acetate 1:1 to 0:1) to afford the title compound as a yellow viscous oil (5.67 g, 97.1%) with a positive ion ESI (M+H)+375.2.

출처