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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2183655생성일: 2026년 10월 26일

Phenyltrimethylammonium bromide dibromide → 1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-one

https://huagongshe.com/reaction/2183655

반응식

참여 물질

역할이름HCID투입량
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
반응물1-(Benzo[b]thiophen-7-yl)propan-1-oneHCID 22473897—
용매TetrahydrofuranHCID 8028—
생성물1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-oneHCID 22474143112.5%

반응 단계

Phenyltrimethylammonium tribromide (1.52 g) was added in portions under nitrogen at 0° C. over 30 minutes to a stirred solution of 1-(benzo[b]thiophen-7-yl)propan-1-one (0.77 g) in tetrahydrofuran (110 ml), then the mixture was stirred at ambient temperature for 18 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added and the mixture was heated under reflux for 4 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added, then the mixture was heated under reflux for 90 minutes, cooled to ambient temperature and filtered. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica using a 7:3 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 1-(benzo[b]thiophen-7-yl)-2-bromopropan-1-one (0.71 g) as an oil which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06900216B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-8f8daf008bb5407a9b9d5c9062fb3418
출처 메모uspto-grants-2005_05