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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 362257생성일: 2026년 10월 26일

1-(1-Benzofuran-3-yl)ethan-1-one → 1-(Benzofuran-3-yl)-2-bromoethanone

https://huagongshe.com/reaction/362257

반응식

참여 물질

역할이름HCID투입량
반응물1-(1-Benzofuran-3-yl)ethan-1-oneHCID 11286612—
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
용매TetrahydrofuranHCID 8028—
생성물1-(Benzofuran-3-yl)-2-bromoethanoneHCID 277658027.4%

반응 단계

A solution of phenyltrimethylammonium tribromide (2.47 g) in tetrahydrofuran (20 ml) was added dropwise at ambient temperature under nitrogen over 5 minutes to a stirred solution of 3-acetylbenzo[b]furan (1 g) in tetrahydrofuran (20 ml), then the mixture was stirred at ambient temperature for a further 1.5 hours, filtered, and the solvent removed in vacuo. The residue was triturated with ether, and the resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(2-bromoacetyl)benzo[b]furan as an off-white solid (0.25 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05869492
출처 데이터셋uspto-grants-1999_02
ORD IDord-10b5b665c38b46309fa8f6f6837d9876
출처 메모uspto-grants-1999_02