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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| 반응물 | 1-(4'-Fluoronaphth-1-yl)-3-methylbutan-1-one | HCID 59796876 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07429607B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-da0f4d5ea2dc42be965ecf9c6fdc8f16 |
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| 출처 메모 | uspto-grants-2008_09 |
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