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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

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyltrimethylammonium bromide dibromideHCID 17977687—
反応物1-(4'-Fluoronaphth-1-yl)-3-methylbutan-1-oneHCID 59796876—
溶媒TetrahydrofuranHCID 8028—
生成物2-Bromo-1-(4-fluoronaphthalen-1-yl)-3-methylbutan-1-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429607B2
出典データセットuspto-grants-2008_09
ORD IDord-da0f4d5ea2dc42be965ecf9c6fdc8f16
出典メモuspto-grants-2008_09