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HRID 33754作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/33754

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 344084847.4%

反応手順

To a solution of 3-methoxythiophenol (3.75 g, 26.7 mmol) in ether (20 mL) was added oxalyl chloride (3.7 mL, 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 (4.30 g, 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 sodum 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 2.46 g (47%) of 6-methoxy-1-benzothiophene-2,3-dione as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429664B2
出典データセットuspto-grants-2008_09
ORD IDord-7b4b5dc5d57c4724a2802c423685f17d
出典メモuspto-grants-2008_09