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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37832생성일: 2026년 10월 24일

Benzyl Bromide → 2-(Benzyloxy)-1-chloro-4-nitrobenzene

https://huagongshe.com/ko/reaction/37832

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-5-nitrophenolHCID 69264—
용매AcetoneHCID 180—
생성물2-(Benzyloxy)-1-chloro-4-nitrobenzeneHCID 1288193399%

반응 단계

Benzyl bromide (0.6 mL, 5.04 mmol) was added dropwise to a mixture of 2-chloro-5-nitro-phenol (800 mg, 4.61 mmol) and potassium carbonate (1.27 g, 9.22 mmol) in acetone (20 mL) at room temperature and heated at reflux for 2 h. Inorganic salts were filtered off and washed with acetone (20 mL). The combined filtrate and washings were concentrated in vacuo, the resulting residue then being dissolved in ethyl acetate (25 mL) and washed successively with water (2×20 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to yield 2-benzyloxy-1-chloro-4-nitro-benzene (1.20 g, 99%) as a cream solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524705B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c6b6cd300ebe4d5bb2b195e5a8862289
출처 메모uspto-grants-2013_09