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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1500191생성일: 2026년 10월 26일

Sodium t-butoxide → N-[5-[3-[3,5-bis(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidin-1-yl]indan-1-yl]propanamide

https://huagongshe.com/reaction/1500191

반응식

참여 물질

역할이름HCID투입량
반응물Sodium t-butoxideHCID 23676156—
반응물3-[3,5-Bis(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidineHCID 53262186—
반응물N-(5-bromoindan-1-yl)propionic acid amideHCID 59453384—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물N-[5-[3-[3,5-bis(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidin-1-yl]indan-1-yl]propanamideHCID 4537792272.6%

반응 조건

온도100 °C

반응 단계

3-[3,5-bis(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidine (0.46 g) and N-(5-bromo-2,3-dihydro-1H-inden-1-yl)propanamide (0.35 g) were dissolved in toluene and deaeration procedure was performed three times under argon atmosphere. Sodium tert-butoxide (0.25 g), Xantphos (0.05 g) and tris(dibenzylideneacetone)dipalladium (0) (chloroform adduct) (0.03 g) were added to the mixture and heated and stirred at 100° C. under argon atmosphere for 2 hours. The solution was cooled to room temperature and the reaction liquid was diluted with ethyl acetate followed by washing with water and brine. The organic layer was dried over anhydrous magnesium sulfate. The desiccant was filtered and separated, the solvent was evaporated off under reduced pressure, and the residue was purified by a silica gel chromatography to obtain N-(5-{3-[3,5-bis(trifluoromethyl)phenyl]-3-(trifluoro-methyl)pyrrolidin-1-yl}-2,3-dihydro-1H- -inden-1-yl)propanamide (0.51 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206122B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-0f571116a842404e97ff515c87c9012d
출처 메모uspto-grants-2015_12