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HRID 1040381作成日:2026年10月27日

Benzyl Bromide → 5-(Benzyloxy)-2-nitrobenzaldehyde

https://huagongshe.com/reaction/1040381

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒DimethylformamideHCID 6228—
生成物5-(Benzyloxy)-2-nitrobenzaldehydeHCID 3849835—

反応手順

To a suspension of 5-hydroxy-2-nitrobenzaldehyde (300 mg, 1.80 mmol), potassium carbonate (498 mg, 3.60 mmol), and tetrabutylammonium iodide (66 mg, 0.18 mmol) in 1.8 mL of dry N,N-dimethylformamide was added benzyl bromide (0.32 mL, 2.7 mmol) at 0° C. After being stirred at room temperature until the starting material disappeared (5 h), the reaction mixture was filtered to remove inorganic salts. The filtrate was diluted with diethyl ether, and the solution was washed with water, saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=90/10 to 75/25) to obtain the title compound as a slightly yellow solid (405 mg, 87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552220B2
出典データセットuspto-grants-2013_10
ORD IDord-ecea00dc8af24c10a89f28789974b9a3
出典メモuspto-grants-2013_10