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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1067413생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1067413

반응식

참여 물질

역할이름HCID투입량
반응물1-BenzoylnaphthaleneHCID 69503—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Naphthalen-2-yl(phenyl)methanolHCID 57077295.3%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06248766B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-0d05bf188d5f495ab3d5b939b0fc3e73
출처 메모uspto-grants-2001_06