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HRID 1067413作成日:2026年10月26日

1-Benzoylnaphthalene → Naphthalen-2-yl(phenyl)methanol

https://huagongshe.com/reaction/1067413

反応式

関与物質

役割名称HCID仕込み量
反応物1-BenzoylnaphthaleneHCID 69503—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Naphthalen-2-yl(phenyl)methanolHCID 57077295.3%

反応手順

To a solution of benzoylnaphthalene (5.00 g, 21.5 mmol) in methanol (30 mL) was added sodium borohydride (400 mg, 10.8 mmol) with ice-cooling and the mixture was stirred at room temperature for 30 minutes. This reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water, dried over MgSO4, and filtered and the filtrate was concentrated under reduced pressure to provide 4.80 g of (2-naphthyl)phenylmethanol. To a solution of this compound (4.80 g, 20.5 mmol) in diisopropyl ether (30 mL) was added phosphorus tribromide (3.70 g, 13.7 mmol) with ice-cooling and the mixture was stirred at room temperature for 1 hour. This reaction mixture was diluted with water and extracted with diisopropyl ether. The organic layer was washed with water and saturated aqueous sodium hydrogen carbonate solution, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure and the solid residue was recrystallized from diisopropyl ether-hexane to provide 4.10 g of the title compound. Yield 64%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06248766B1
出典データセットuspto-grants-2001_06
ORD IDord-0d05bf188d5f495ab3d5b939b0fc3e73
出典メモuspto-grants-2001_06