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HRID 1795113作成日:2026年10月24日

1-Chloromethylnaphthalene → 2-(Naphthalen-1-ylmethoxy)benzaldehyde

https://huagongshe.com/ja/reaction/1795113

反応式

関与物質

役割名称HCID仕込み量
反応物1-ChloromethylnaphthaleneHCID 6845—
反応物SalicylaldehydeHCID 6998—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(Naphthalen-1-ylmethoxy)benzaldehydeHCID 88549643.2%

反応条件

温度100 °C

反応手順

To a solution of 2-hydroxybenzaldehyde (2.30 g, 18.8 mmol) in DMF (20 mL) is added 1-(chloromethyl)-naphthalene (3.36 mL, 22.6 mmol) and K2CO3 (3.11 g, 22.6 mmol), and the reaction mixture is heated to 100° C. for 12 h. Once complete, the reaction mixture is cooled to room temperature and diluted with water (100 mL) prior to being poured into a separatory funnel containing ethyl acetate (250 mL). The organic layer is separated, washed with brine (2×) and dried over sodium sulfate prior to concentration. The crude product is purified by column chromatography (5% ethyl acetate in hexanes) to afford 2-(1-naphthylmethoxy)benzaldehyde (2.13 g, 43%) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07026339B2
出典データセットuspto-grants-2006_04
ORD IDord-3f39b2fc764a4dc582d690e962a26da4
出典メモuspto-grants-2006_04