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HRID 1610600作成日:2026年10月27日

Benzyl 4-Hydroxybenzoate → Benzyl 4-(pyridin-3-yloxy)benzoate

https://huagongshe.com/reaction/1610600

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 4-HydroxybenzoateHCID 7180—
反応物3-BromopyridineHCID 12286—
反応物Potassium tert-butoxideHCID 23665647—
触媒CopperHCID 23978—
溶媒DimethylformamideHCID 6228—
生成物Benzyl 4-(pyridin-3-yloxy)benzoateHCID 22262109—

反応手順

To a solution of benzyl 4-hydroxybenzoate (25.0 g, 110 mmol) in N,N-dimethylformamide (60 ml) was added potassium tert-butoxide (12.3 g, 110 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was evaporated under reduced pressure, and 3-bromopyridine (25.0 g, 110 mmol), a copper powder (1.76 g, 27.2 mmol) and N,N-dimethylformamide (80 ml) were added. The mixture was stirred at 120° C. for 8 hrs. The reaction solution was filtered with celite and the filtrate was evaporated under reduced pressure. To the residue was added water (500 ml) and the mixture was extracted with ethyl acetate (500 ml). The extract was washed successively with water and saturated brine, dried (anhydrous magnesium sulfate) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1-2:1) to give the objective substance (18.0 g, 54%, crude).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06982348B2
出典データセットuspto-grants-2006_01
ORD IDord-3fadcb0b6113453aac7fa19ac40d1eab
出典メモuspto-grants-2006_01