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HRID 1864611作成日:2026年10月27日

Oxalyl chloride → 6-Methoxy-1-benzothiophene-2,3-dione

https://huagongshe.com/reaction/1864611

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物3-MethoxybenzenethiolHCID 84989—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒Diethyl EtherHCID 3283—
生成物6-Methoxy-1-benzothiophene-2,3-dioneHCID 344084847%

反応手順

To a solution of 3-methoxythiophenol (26.7 mmol) in ether (20 mL) was added oxalyl chloride (43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodium bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 6-methoxy-1-benzothiophene-2,3-dione (47%) as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07625924B2
出典データセットuspto-grants-2009_12
ORD IDord-d28adc8a888f4d9b8bea1d56c6e9dc3a
出典メモuspto-grants-2009_12