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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 435143생성일: 2026년 10월 25일

N-bromobutanimide → Methyl 4-(bromomethyl)-3-nitrobenzoate

https://huagongshe.com/reaction/435143

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Methyl 4-methyl-3-nitrobenzoateHCID 81816—
용매Carbon TetrachlorideHCID 5943—
생성물Methyl 4-(bromomethyl)-3-nitrobenzoateHCID 13399987—

반응 단계

All of the 4-methoxycarbonyl-2-nitrotoluene obtained as described above was dissolved in carbon tetrachloride. Approximately 14.2 g (0.082 mole) of N-bromosuccinimide was added to the carbon tetrachloride solution. The resulting solution was heated to reflux temperature and stirred for approximately 64 hours. The solution was cooled and the succinimide was removed by vacuum filtration. The remaining solution was concentrated on a rotary evaporator using water aspirator vacuum. The synthesis produced 24 g of 4-methoxycarbonyl-2-nitrobenzyl bromide. The cholate ester of this product was then prepared as described for the preparation of the esters in Section B. The O,O,O-triacetyl derivative was also prepared as described in Section F.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04400461
출처 데이터셋uspto-grants-1983_08
ORD IDord-2098fbb8c47a4459a83564039f42c795
출처 메모uspto-grants-1983_08