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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1465453생성일: 2026년 10월 26일

4'-Bromoacetanilide → 4-bromo-N-ethylaniline

https://huagongshe.com/reaction/1465453

반응식

참여 물질

역할이름HCID투입량
반응물4'-BromoacetanilideHCID 7683—
반응물Sodium HydroxideHCID 14798—
반응물Sodium SulfateHCID 24436—
반응물Aluminium lithium hydrideHCID 21226445—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-bromo-N-ethylanilineHCID 1174565695%

반응 단계

To a suspension of lithium aluminum hydride (1.1 g, 29 mmol) in anhydrous tetrahydrofuran (70 ml) was added dropwise at 0° C. a solution of N-(4-bromophenyl)acetamide (2.5 g, 12 mmol) in anhydrous tetrahydrofuran (30 ml). The reaction mixture was warmed to room temperature, and stirred for 15 mins. After further stirring at 60° C. for 2 hrs, the mixture was cooled to 0° C. Water (1.8 ml) was added dropwise by small portions, and 2M aqueous sodium hydroxide solution (1.55 ml) was added dropwise. After stirring for 15 mins, sodium sulfate was added, and the mixture was further stirred for 15 mins. The mixture was filtered through a Celite pad, and the insoluble material was washed with dichloromethane. The filtrate and washing solution were combined and concentrated under reduced pressure to give 4-bromo-N-ethylaniline (2.28 g, yield 95%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08999989B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-32d094858c69455c9e79d060f77bebd9
출처 메모uspto-grants-2015_04