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HRID 33578作成日:2026年10月26日
Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-one
https://huagongshe.com/reaction/33578
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| 反応物 | 1-(4'-Fluoronaphth-1-yl)-3-methylbutan-1-one | HCID 59796876 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-one | HCID 59796873 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07429607B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-da0f4d5ea2dc42be965ecf9c6fdc8f16 |
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| 出典メモ | uspto-grants-2008_09 |
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