Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662713생성일: 2026년 10월 24일
Water → tert-butyl (2S,4R)-4-(3-{[tert-butyl(dimethyl)silyl]oxy}propoxy)-2-[(dimethylamino)carbonyl]pyrrolidine-1-carboxylate
https://huagongshe.com/ko/reaction/1662713
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | HCID 15261805 | HCID 15261805 | — |
| 반응물 | tert-butyl (2S,4S)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate | HCID 67430109 | — |
| 생성물 | tert-butyl (2S,4R)-4-(3-{[tert-butyl(dimethyl)silyl]oxy}propoxy)-2-[(dimethylamino)carbonyl]pyrrolidine-1-carboxylate | HCID 67429248 | — |
반응 단계
Under nitrogen atmosphere, to a suspension of 1.55 g of NaH in THF (100 ml) was added 10.0 g of tert-butyl (2S,4S)-2-[(dimethylamino)carbonyl]-4-hydroxypyrrolidine-1-carboxylate and the reaction mixture was stirred at 50° C. for one hour. Thereafter, at the same temperature, solution of 23.2 g of (3-iodopropyl)-tert-butyl-dimethyl silane in THF (10 ml) was added, and the solution was refluxed for two hours. The solution was poured into water and the resulting mixture was extracted with EtOAc; the organic layer was washed with saturated brine and dried over MgSO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N; mobile phase: n-hexane/EtOAc=1/1 to 0/1; v/v) to obtain 2.10 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08030499B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-ef4262beb1b746b1a18a80a9c364d842 |
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| 출처 메모 | uspto-grants-2011_10 |
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