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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133545생성일: 2026년 10월 24일

Acetic Anhydride → N-(3-benzoyl-5-bromo-thiophen-2-yl) acetamide

https://huagongshe.com/ko/reaction/133545

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물N-bromobutanimideHCID 67184—
반응물(2-Aminothiophen-3-yl)(phenyl)methanoneHCID 644720—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물N-(3-benzoyl-5-bromo-thiophen-2-yl) acetamideHCID 1664023153.3%

반응 단계

To a stirred solution of 1.00 g (4.92 mmol) of (2-amino-thiophen-3-yl)-phenyl-methanone (the preparation of which is described in example 20) in 20 ml CFCl2 at 0° C. was added 0.92 g (5.18 mmol) NBS (N-bromo succinimide) in one portion. After 10 minutes, 4.65 ml (49.2 mmol) of acetic anhydride, 0.68 ml (4.92 mmol) of Et3N and 0.30 g (2.45 mmol) of DMAP were added. Stirring was continued at RT for 2 hours, the mixture was poured onto water and extracted three times with CH2Cl2. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (heptane/CH2Cl2 1:1) afforded 0.85 g (53%) N-(3-benzoyl-5-bromo-thiophen-2-yl)-acetamide as a light brown solid. ES-MS m/e (%): 324, 326 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390903B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-7024b35b3d4e45ab9107f3a2c86fa6c9
출처 메모uspto-grants-2008_06