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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2608생성일: 2026년 10월 24일

2-Methylthiophene → 1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene

https://huagongshe.com/ko/reaction/2608

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참여 물질

역할이름HCID투입량
반응물2-MethylthiopheneHCID 11126—
반응물7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Diethylether ethylacetateHCID 21584169—
생성물1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthaleneHCID 1862006262.3%

반응 조건

온도0 °C

반응 단계

To a cold (-78° C.) solution of 2-methylthiophene (800 mg, 8.1 mmol) in THF (10 mL) was added n-BuLi (1.6M solution in hexane, 5 mL). The mixture was stirred for 1.5 hours and transferred to a cold (-78° C.) flask containing 3,4-dihydro-4,4-dimethyl-7-bromo-1(2H)-naphthalenone (Compound A, 1.63 g, 6.5 mmol), in THF (15 mL). The mixture was gradually warmed to 0° C. The reaction mixture was diluted with ether:ethylacetate (1:1, 80 mL), washed with water (10 mL), brine (10 mL), dried with MgSO4 and the solvent was removed by evaporation. The crude material was dissolved in dichloroethane (20 mL) and pTSA (40 mg) was added. The mixture was stirred at ambient temperature for 16 hours and at 50° C. for 4 hours. The reaction mixture was diluted with ether (150 mL), washed with aqueous 10% NaHCO3 (10 mL), brine (10 mL) and dried with MgSO4. Purification by chromatography on silica gel gave 1.35 g of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728846
출처 데이터셋uspto-grants-1998_03
ORD IDord-1181981a49704b02b7381620902d58eb
출처 메모uspto-grants-1998_03