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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22868생성일: 2026년 10월 24일

Formic Acid → Formamide, N-(4-bromophenyl)-

https://huagongshe.com/ko/reaction/22868

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참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물4-BromoanilineHCID 7807—
반응물Acetic AnhydrideHCID 7918—
용매TetrahydrofuranHCID 8028—
생성물Formamide, N-(4-bromophenyl)-HCID 1747499.2%

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온도0 °C

반응 단계

A 5-Liter round bottom flask was charged with acetic anhydride (488 mL, 5.2 mol) and cooled to 0° C. Formic acid (240 mL, 6.4 mol) was then added at a rate that did not elevate the temperature of the reaction mixture above 10° C. After the formic acid was added, the temperature of the reaction was raised to 50-60° C. and stirred for 3 hours. The reaction was then cooled to 0° C. and 400 mL of THF was added. A solution of 4-bromoaniline (344 g, 2.0 mol) in 800 mL of THF was added dropwise. After the addition was complete, the reaction was allowed to stir at this temperature for 4 hours. The reaction was checked by thin-layer chromatography and found to be complete. The reaction mixture was transferred to a round bottom flask and the solvent was removed in vacuo. When the solvent had been removed, the residue crystallized. The solid was triturated with heptane and filtered. Obtained 396.8 grams of desired N-(4-bromo-phenyl)-formamide. Yield 99.2% The spectral properties of the solid were consistent with the desired material. Step (2): (4-bromo-phenyl)-methyl-amine

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849648B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-46bb61989247402b83f957372f1f9da2
출처 메모uspto-grants-2005_02