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HRID 54972作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物1-Bromo-2-methylnaphthaleneHCID 75754—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物(2-Methyl-1-naphthyl)(phenyl)methanolHCID 1995712078.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624922
出典データセットuspto-grants-1997_04
ORD IDord-0c4660183fbc41969b1652484277c365
出典メモuspto-grants-1997_04