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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033583생성일: 2026년 10월 26일

N-bromobutanimide → Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate

https://huagongshe.com/reaction/1033583

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물ethyl 4-(4-chlorophenyl)-1H-pyrrole-3-carboxylateHCID 470434—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylateHCID 1501018590,348.398%

반응 단계

Ethyl 4-(p-chlorophenyl)pyrrole-3-carboxylate (1.6 g., 0.0064 mmol) is dissolved in tetrahydrofuran (40 mL). N-bromosuccinimide (1.14 g., 0.0064 mmol) is added in small portions at 25°-28° C. After the addition is complete, the solution is stirred overnight at room temperature. The solution is concentrated in vacuo and the solid residue partioned between water and ether. The ether layer is separated and dried over magnesium sulfate. Work-up of the ether extract leaves 1.9 g (90%) of a white solid which is purified by stirring with a mixture of 80/20 hexane/ethyl acetate. The insoluble solid (1.3 g, 62%) is collected and has m.p. 161°-164° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310938
출처 데이터셋uspto-grants-1994_05
ORD IDord-ad8d558a86874856becc73421c1a1ec8
출처 메모uspto-grants-1994_05