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HRID 1862747作成日:2026年10月26日

2-Methylthiophene → 2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene

https://huagongshe.com/reaction/1862747

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylthiopheneHCID 11126—
反応物6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-eneHCID 86191489—

反応手順

To a cold (−78° C.) solution of 2-methylthiophene (1.2 g, 12.2 mmol) in THF (8 mL) was added n-BuLi in hexane (1.6M, 8.5 mL). The mixture was warmed to ambient temperature over 30 minutes. with stirring. The mixture was recooled to −78° C. and a solution of 2,2-dimethyl-6-bromo-thiochroman4-one (Compound M, 1.4 g, 5.2 mmol) in THF (10 mL) was added. The mixture was stirred for 16 hours at ambient temperature. Then the reaction mixture was diluted with ether (125 mL), washed with water (10 mL), brine (10 mL) dried and the solvent was removed by evaporation. The product was seperated by column chromatography and was dissolved in dichloromethane (5 mL). To this solution p-TSA (5 mg) was added and the mixture was stirred at ambient temperature for 5 min. The reaction was quenched with 10% NaHCO3 (3 mL), washed with brine (5 mL), dried and the solvent was removed by distillation. The residual crude a material was purified by column chromatography to obtain the title compound as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06538149B1
出典データセットuspto-grants-2003_03
ORD IDord-bc2cee50cb7c4f00b25806ff839b49f0
出典メモuspto-grants-2003_03