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HRID 1909093作成日:2026年10月26日

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

https://huagongshe.com/reaction/1909093

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物4-[4-(Trifluoromethoxy)phenoxy]piperidineHCID 16115439—
反応物Sodium t-butoxideHCID 23676156—
反応物4-[(4-Bromophenoxy)methyl]-2,2,4-trimethyl-1,3-dioxolaneHCID 71059331—
触媒palladium(II) acetateHCID 167845—
触媒Tri-tert-butylphosphine tetraphenylborateHCID 86674235—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-[4-(Trifluoromethoxy)phenoxy]-1-{4-[(2,2,4-trimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}piperidineHCID 6736112493.2%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08598358B2
出典データセットuspto-grants-2013_12
ORD IDord-d3bee796665b41afb7076e2b8902854f
出典メモuspto-grants-2013_12