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HRID 563453作成日:2026年10月25日

Dimethyl Sulfoxide → 1-Bromo-2-methoxynaphthalene

https://huagongshe.com/reaction/563453

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Methyl iodideHCID 6328—
反応物1-Bromo-2-naphtholHCID 11316—
反応物Potassium HydroxideHCID 14797—
溶媒WaterHCID 962—
生成物1-Bromo-2-methoxynaphthaleneHCID 7286069%

反応手順

A 500 mL three-necked round-bottomed flask was charged with 1-bromonaphthalen-2-ol (30.0 g, 134.5 mmol), potassium hydroxide (KOH) (11.3 g, 201.7 mmol) and DMSO (300 mL), and the mixture was stirred under nitrogen atmosphere for 10 minutes, After cooling the mixture by using ice-water bath, iodomethane (28.6 g, 201.7 mmol) was slowly added dropwise thereto. Then, the resultant mixture was stirred under nitrogen atmosphere at ambient temperature for 12 hours, and then at 50° C. for 1 hour. After cooling to ambient temperature, the reaction mixture was mixed with water (500 mL), and extracted with diethyl ether. Organic mixture was washed three times with distilled water, and dried over anhydrous magnesium sulfate (MgSO4). After removing the solvent by using a rotary evaporator, the residue was purified via silica gel column chromatography (eluent: n-hexane) to obtain 1-bromo-2-methoxynaphthalene (22.0 g, yield: 69.0%) as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067511B2
出典データセットuspto-grants-2011_11
ORD IDord-5f3bba70d52444a189792b56345d99b6
出典メモuspto-grants-2011_11