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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1773973생성일: 2026년 10월 27일

N-bromobutanimide → Ethyl 2-(4-amino-3-bromophenyl)acetate

https://huagongshe.com/reaction/1773973

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물p-Aminophenylacetic acid ethyl esterHCID 225219—
용매AcetonitrileHCID 6342—
생성물Ethyl 2-(4-amino-3-bromophenyl)acetateHCID 19702145—

반응 단계

To a solution of ethyl 4-aminophenylacetate (1.79 g, 10 mmol, 1 eq.) in MeCN (50 mL), N-bromsuccinimide (1.78 g, 10 mmol, 1 eq.) was added slowly. The mixture was stirred at r.t. for 72 hours. The reaction mixture was concentrated in vacuo. The residue was partitioned between water (50 mL) and Et2O (50 mL). The org. phase was washed with sat. aq. NaCl soln. (1×50 mL), dried over MgSO4, and concentrated in vacuo to give (4-amino-3-bromo-phenyl)-acetic acid ethyl ester as an orange oil. The product was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09255090B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-e986737d4dab4274bb71e2f7d4a0cac2
출처 메모uspto-grants-2016_02