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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1754980생성일: 2026년 10월 23일

Ammonium Chloride → Ethyl 4-(3,3,3-trifluoro-propylidene)-cyclohexanecarboxylate

https://huagongshe.com/ko/reaction/1754980

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 4-oxocyclohexanecarboxylateHCID 317638—
반응물Triphenyl(3,3,3-trifluoropropyl)phosphanium iodideHCID 19694095—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-(3,3,3-trifluoro-propylidene)-cyclohexanecarboxylateHCID 6681760796%

반응 단계

n-Butyllithium (1.6 M solution in hexane, 26 ml, 41.6 mmol) was added to a solution of triphenyl-(3,3,3-trifluoro-propyl)-phosphonium iodide (20.25 g, 41.64 mmol) in THF (141 ml) at −78° C. over 13 minutes, and the mixture was stirred at the same temperature for 20 minutes. A solution of 4-oxo-cyclohexanecarboxylic acid ethyl ester (6.56 g, 38.54 mmol) in THF (22 ml) was added to the reaction solution at −78° C. over 17 minutes, and the mixture was stirred at the same temperature for one hour. A 50% saturated aqueous ammonium chloride solution was added, followed by extraction with dichloromethane. The organic layer was then dried over MgSO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give ethyl 4-(3,3,3-trifluoro-propylidene)-cyclohexanecarboxylate (9.25 g, 96%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09169254B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-41355dc934384b049f88857382137aa4
출처 메모uspto-grants-2015_10