Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1750533생성일: 2026년 10월 27일
tert-butyl N-(2-oxocyclopentyl)carbamate → tert-Butyl N-[(2E)-2-{[5-(trifluoromethyl)pyridin-2-yl]methylidene}cyclopentyl]carbamate
https://huagongshe.com/reaction/1750533
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | tert-butyl N-(2-oxocyclopentyl)carbamate | HCID 357962 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | Diethyl ((5-(trifluoromethyl)pyridin-2-yl)methyl)phosphonate | HCID 118320757 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl N-[(2E)-2-{[5-(trifluoromethyl)pyridin-2-yl]methylidene}cyclopentyl]carbamate | HCID 118308075 | — |
반응 단계
To the suspension of diethyl ((5-(trifluoromethyl)pyridin-2-yl)methyl)phosphonate (2.0 g, 6.71 mmol) in THF (50 ml) at 0° C. was added potassium tert-butoxide (1.5 g, 13.42 mmol) and then stirred at room temperature for 30 minutes. To this was then added a solution of tert-butyl N-(2-oxocyclopentyl)carbamate (CAS number 477585-30-1; 1.62 g, 8.05 mmol) in THF (20 ml) and the resulting reaction was stirred at room temperature for 1 hour and then heated at reflux overnight. The reaction was quenched with water (50 ml) and extracted with ethyl acetate (3×100 ml). The combined organics were washed with brine, dried over sodium sulfate and concentrated in vacuo. The resulting residue was purified by column chromatography (silica, 0-15% ethyl acetate/n-hexane) to afford the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09156829B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-0960129e8ec84276924b2a52d92131e0 |
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| 출처 메모 | uspto-grants-2015_10 |
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