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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384400생성일: 2026년 10월 26일

N-bromobutanimide → Methyl 5-bromo-2-methylfuran-3-carboxylate

https://huagongshe.com/reaction/384400

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Methyl 2-methylfuran-3-carboxylateHCID 80237—
촉매AzobisisobutyronitrileHCID 6547—
용매TolueneHCID 1140—
생성물Methyl 5-bromo-2-methylfuran-3-carboxylateHCID 1553419061%

반응 조건

온도0 °C

반응 단계

2-Methyl-furan-3-carboxylic acid methyl ester (2.0 g, 14.3 mmol) was dissolved in toluene followed by addition of 2,2′-azobis(2-methylpropionitrile) (10 mg, 0.06 mmol). The mixture was cooled to 0° C. by an ice-water bath followed by addition of N-bromosuccinimide (2.8 g, 15.7 mmol). Upon completion of the addition, the ice-water bath was removed and the reaction mixture was stirred at room temperature overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 5-bromo-2-methyl-furan-3-carboxylic acid methyl ester 53a (1.9 g, yield 61%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367710B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-cc09c0e355394ac299b72b7d79f62f71
출처 메모uspto-grants-2013_02