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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54972생성일: 2026년 10월 24일

Benzaldehyde → (2-Methyl-1-naphthyl)(phenyl)methanol

https://huagongshe.com/ko/reaction/54972

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물1-Bromo-2-methylnaphthaleneHCID 75754—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물(2-Methyl-1-naphthyl)(phenyl)methanolHCID 1995712078.7%

반응 단계

A solution of 10 g (45 mmol) of 1-bromo-2-methylnaphthalene in 75 mL of THF was refluxed with 1.2 g (50 mmol) of magnesium turnings for three hours. The reaction was cooled on ice and 4.8 mL (43 mmol) of benzaldehyde was added. The ice was removed, the reaction was stirred 45 minutes and quenched with 5 mL of 1N HCl followed by 50 mL of water. The reaction was extracted into ethyl acetate, dried over sodium sulfate and flash chromatographed through silica gel with 5-10% ethyl acetate in hexane to provide 8.4 g (75%) of 2-methyl-a-phenyl-1-naphthalenemethanol as a pale yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624922
출처 데이터셋uspto-grants-1997_04
ORD IDord-0c4660183fbc41969b1652484277c365
출처 메모uspto-grants-1997_04