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HRID 493097作成日:2026年10月26日

2-Methylbenzo(b)thiophene → 2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/493097

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbenzo(b)thiopheneHCID 70952—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物2-(Methoxycarbonyl)phenyl sulfenyl chlorideHCID 12223537—
溶媒1,2-DichloroethaneHCID 11—
生成物2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl esterHCID 68898083—

反応条件

温度0 °C

反応手順

2-(Methoxycarbonyl)phenyl sulfenyl chloride (10 mL 0.29 M solution in 1,2-dichloro-ethane, 2.9 mmol) is added to a solution of 2-methyl-benzo[b]thiophene (445 mg, 3mmol) in 5 mL 1,2-dichloro-ethane. The reaction mixture is cooled to 0° C. Aluminium chloride (400 mg, 3 mmol) is added and the reaction mixture is stirred for 4 hours at room temperature. The reaction is quenched with water. The organic phase is washed with brine, dried with MgSO4 and concentrated in vacuo. The residue is purified by flash chromatography on silica gel using ethyl acetate-heptane as eluent. This furnishes 651 mg (69%) of the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534791B2
出典データセットuspto-grants-2009_05
ORD IDord-7f52d5d71db94ef4b42538e74fd4c716
出典メモuspto-grants-2009_05