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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883073생성일: 2026년 10월 26일

Diethyl Ether → 7-(5-Acetyl-2-trifluoromethoxy-phenyl)-1-ethyl-4,4,6-trimethyl-3,4-dihydro-1h-quinolin-2-one

https://huagongshe.com/reaction/883073

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물TriacetoxyperiodinaneHCID 159087—
반응물3-(1-Ethyl-4,4,6-trimethyl-2-oxo-1,2,3,4-tetrahydro-quinolin-7-yl)-4-trifluoromethoxy-benzaldehydeHCID 11223449—
반응물HCID 178418573HCID 178418573—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물7-(5-Acetyl-2-trifluoromethoxy-phenyl)-1-ethyl-4,4,6-trimethyl-3,4-dihydro-1h-quinolin-2-oneHCID 6866634775%

반응 단계

A solution of Compound 2A (270 mg, 0.66 mmol) in 3 mL of dry THF was cooled to −78° C. and treated with a 3M solution of methyl magnesium bromide in ether (0.24 mL, 0.73 mmol). The reaction mixture was allowed to slowly warm to room temperature where it was quenched with 10 mL of a saturated ammonium chloride solution. The reaction mixture was then passed through a 10 mL SPE (solid phase extraction) column which was further washed with dichloromethane. The eluant was collected and stripped to give crude alcohol which was then dissolved in dichloromethane and treated with Dess-Martin reagent (336 mg, 0.79 mmol) and stirred at room temperature overnight. The reaction was quenched with 4 mL of saturated sodium thiosulfate solution and 4 mL of saturated sodium bicarbonate solution, the reaction mixture was stirred until clear. The reaction mixture was passed through another SPE and eluted with dichloromethane, removal of solvent yielded crude ketone which was purified with flash chromatography (25% EtOAc/hexane) to yield 207 mg (75%) of the desired product (Compound 19A) and a white solid. MS (electrospray): mass calculated for C23H24F3NO3, 419.17; m/z found 420.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08236819B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-47d8fcc97d284dd3937d91c261d965f2
출처 메모uspto-grants-2012_08