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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33578생성일: 2026년 10월 25일

Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-one

https://huagongshe.com/reaction/33578

반응식

참여 물질

역할이름HCID투입량
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
반응물1-(4'-Fluoronaphth-1-yl)-3-methylbutan-1-oneHCID 59796876—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-oneHCID 59796873—

반응 단계

To a solution of 3-methyl-1-(4′-fluoronaphth-1-yl)butan-1-one (7 g) in anhydrous tetrahydrofuran (80 ml) was added phenyltrimethylammonium tribromide (11.5 g). The resulting mixture was stirred overnight at ambient temperature then partitioned between petroleum ether and water. The organic layer was separated, washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo to yield crude 2-bromo-1-(4′-fluoronaphth-1-yl)-3-methylbutan-1-one. Sodium acetate (2.75 g) and anhydrous dimethylformamide (30 ml) were added and the resulting mixture was stirred at 80° C. for 5 hours. After cooling, the mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted once with ethyl acetate. The combined organic layers were washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo. The title compound (4.8 g) was obtained following silica gel column chromatography of the residue in 30-100% dichloromethane in petroleum ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429607B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-da0f4d5ea2dc42be965ecf9c6fdc8f16
출처 메모uspto-grants-2008_09