Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5070생성일: 2026년 10월 26일
Sodium Iodide → (2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidine
https://huagongshe.com/reaction/5070
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 2-Fluoroethyl bromide | HCID 12982 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-pyrrolidine | HCID 14880267 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidine | HCID 10781417 | — |
반응 단계
0.4 ml of 1-bromo-2-fluoroethane, 3.83 g of sodium iodide and 0.38 g of sodium bicarbonate were added to a solution of 1.2 g of (2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine dissolved in 12 ml of dry dimethylformamide, whilst ice-cooling, and the mixture was stirred at room temperature for 20 minutes and then at 40° C. for 20 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was subjected to column chromatography through silica gel (Katayama Chemicals Industries Co., silica gel 60K070). 838 mg of the title compound, melting of 122°-123° C., were obtained as a powder from those fractions eluted with ethyl acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05242914 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-968f75398c654623b4623e870b77110f |
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| 출처 메모 | uspto-grants-1993_09 |
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