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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1909093생성일: 2026년 10월 25일

Toluene → 4-[4-(Trifluoromethoxy)phenoxy]-1-{4-[(2,2,4-trimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}piperidine

https://huagongshe.com/reaction/1909093

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물4-[4-(Trifluoromethoxy)phenoxy]piperidineHCID 16115439—
반응물Sodium t-butoxideHCID 23676156—
반응물4-[(4-Bromophenoxy)methyl]-2,2,4-trimethyl-1,3-dioxolaneHCID 71059331—
촉매palladium(II) acetateHCID 167845—
촉매Tri-tert-butylphosphine tetraphenylborateHCID 86674235—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-[4-(Trifluoromethoxy)phenoxy]-1-{4-[(2,2,4-trimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}piperidineHCID 6736112493.2%

반응 단계

4-[(4-Bromophenoxy)methyl]-2,2,4-trimethyl-1,3-dioxolane (156 mg, 0.518 mmol), 4-[4-(trifluoromethoxy)phenoxy]piperidine (135 mg, 0.517 mmol), palladium acetate (1.2 mg, 0.0053 mmol), tri-tert-butylphosphine tetraphenylborate (2.7 mg, 0.0052 mmol), sodium tert-butoxide (55 mg, 0.57 mmol), and toluene (2 mL) were mixed and stirred under reflux for 2 hours. Ethyl acetate and water were added to the reaction mixture, followed by extraction. The organic layer was washed with water twice. A residue was obtained by concentrating the organic layer under reduced pressure, and the resulting residue was then subjected to chromatography refining (methylene chloride) using silica gel, obtaining 232 mg of the objective compound (yield: 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598358B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-d3bee796665b41afb7076e2b8902854f
출처 메모uspto-grants-2013_12