反応 #51864

反応方程式

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

収率 97.1%

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

収率 97.1%

溶媒

dimethylformamide

反応条件

後処理

1. 1
   workup.STIRRINGThe mixture was stirred for 16 hours at ambient temperature
2. 2
   抽出extracted with ethyl acetate (3×150 cm3)
3. 3
   洗浄The combined ethyl acetate extracts were washed with water (2×100 cm3), brine (1×100 cm3)
4. 4
   乾燥dried over sodium sulfate, vacuum
5. 5
   ろ過filtered
6. 6
   その他the volatile fractions removed in vacuo to a foul smelling yellow oil
7. 7
   その他The crude product was purified by column chromatography (silica, eluting with hexane-ethyl acetate 1:1 to 0:1)

実験手順

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.

出典