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HRID 2623생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2623

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylthiopheneHCID 11126—
반응물6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-eneHCID 86191489—

반응 단계

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-thiochroman-4-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 material was purified by column chromatography to obtain the title compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728846
출처 데이터셋uspto-grants-1998_03
ORD IDord-4ced6f59ef644dca80ccd38e6f9bbbd4
출처 메모uspto-grants-1998_03