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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1040381생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1040381

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
촉매Tetrabutylammonium IodideHCID 67553—
용매DimethylformamideHCID 6228—
생성물5-(Benzyloxy)-2-nitrobenzaldehydeHCID 3849835—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552220B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-ecea00dc8af24c10a89f28789974b9a3
출처 메모uspto-grants-2013_10