돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1678709생성일: 2026년 10월 26일

N-bromobutanimide → 1-(Bromomethyl)-4-methoxy-2-nitrobenzene

https://huagongshe.com/reaction/1678709

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물4-Methyl-3-nitroanisoleHCID 87137—
용매Carbon TetrachlorideHCID 5943—
생성물1-(Bromomethyl)-4-methoxy-2-nitrobenzeneHCID 3747830—

반응 단계

4-Methyl-3-nitroanisole (2.7 mL; manufactured by Sigma-Aldrich Co.) was dissolved in carbon tetrachloride (20 mL; manufactured by Wako Pure Chemical Industries, Ltd.), and NBS (4.0520 g; manufactured by Tokyo Chemical Industry Co., Ltd.) and hydrated benzoyl peroxide (348 mg; manufactured by Sigma-Aldrich Co.) were added to the solution. The mixture was purged with nitrogen, and was stirred for 3 hours at reflux. The reaction solution was filtered, and then the filtrate was washed with an aqueous solution of NaHSO3 and water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=94:6→73:27). Thus, the title compound (3.2549 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008506B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-160003e9764547afa9c7eb3bf7cabab0
출처 메모uspto-grants-2011_08