돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(2-oxocyclopentyl)carbamateHCID 357962—
반응물Potassium tert-butoxideHCID 23665647—
반응물Diethyl ((5-(trifluoromethyl)pyridin-2-yl)methyl)phosphonateHCID 118320757—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl N-[(2E)-2-{[5-(trifluoromethyl)pyridin-2-yl]methylidene}cyclopentyl]carbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156829B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-0960129e8ec84276924b2a52d92131e0
출처 메모uspto-grants-2015_10