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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360253생성일: 2026년 10월 26일

Benzyl Bromide → Methyl 4-benzyloxy-3-nitrobenzoate

https://huagongshe.com/reaction/1360253

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물Benzoic acid, 4-hydroxy-3-nitro-, methyl esterHCID 66835—
용매AcetoneHCID 180—
생성물Methyl 4-benzyloxy-3-nitrobenzoateHCID 289857—

반응 단계

A solution of 4-hydroxy-3-nitro-benzoic acid methyl ester (30 g, 152 mmol) in acetone (1000 mL) was charged into a 2 L reactor and treated with K2CO3 (31.5 g, 228 mol) and benzyl bromide (52 g, 36.1 mL, 304 mmol). The mixture was mechanically stirred at heated at reflux for 16 hours under a light argon flux. After cooling to room temperature the solvent was evaporated. The residue was taken up in ethyl acetate/water and the two phases were separated. The aqueous phase was extracted three times with ethyl acetate (total solvent volume: 1.5 L, total water volume 1 L). The combined organic phases were dried over sodium sulfate and evaporated. 4-Benzyloxy-3-nitro-benzoic acid methyl ester thus obtained was used crude in the following reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879845B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-25a51d2a74f548ab80268e92d12df394
출처 메모uspto-grants-2011_02