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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432169생성일: 2026년 10월 27일

Benzyl chloroformate → benzyl N-(4-bromo-2-methoxyphenyl)carbamate

https://huagongshe.com/reaction/432169

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물4-Bromo-2-methoxyanilineHCID 459257—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물benzyl N-(4-bromo-2-methoxyphenyl)carbamateHCID 2234683774.3%

반응 단계

A solution of sodium bicarbonate (3.12 g, 0.0371 mol) in water (35 mL) was added to a solution of 4-bromo-2-methoxyaniline (3.00 g, 0.0148 mol) in dioxane (50 mL). The resulting mixture was stirred for 5 minutes and benzyl chloroformate (3.8 g, 0.022 mol) was added dropwise over 3 minutes. The reaction mixture was for two hours, then dioxane was removed under reduced pressure and the water phase was extracted twice with ethyl acetate (100 mL each). The combined organic extracts were dried over magnesium sulfate and after filtration concentrated under reduced pressure. The resulting residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (5:95) as mobile phase to yield benzyl N-(4-bromo-2-methoxyphenyl)carbamate (3.75 g, 0.011 mol) as a white solid: 1H NMR (DMSO-d6, 400 MHz) 8.72 (s, 1H), 7.61 (d, 1H), 7.38 (m, 5H), 7.20 (s, 1H), 7.10 (d, 1H), 5.14 (s, 2H), 3.81 (s, 3H). TLC (ethyl acetate/heptane 1:9) Rf 0.21.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660744B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-711581551b3f4498b6a374c6f81df232
출처 메모uspto-grants-2003_12