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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2242290생성일: 2026년 10월 27일

1,2-Dimethoxyethane → 5,5'-Bis[4-(octyloxy)phenyl]-2,2'-bithiophene

https://huagongshe.com/reaction/2242290

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물5,5'-Dibromo-2,2'-bithiopheneHCID 638908—
반응물4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매WaterHCID 962—
생성물5,5'-Bis[4-(octyloxy)phenyl]-2,2'-bithiopheneHCID 59027319—

반응 조건

온도70 °C

반응 단계

To a mixture of 4-octyloxy-phenylboronic acid (Compound 7) (12.0 g, 0.048 mol), 5,5′-dibromo-2,2′-bithiophene (Compound 8) (7.23 g, 0.022 mol), bis(triphenylphosphine) palladium (II) dichloride (0.39 g, 0.56 mmol), and potassium phosphate (15.3 g, 0.072 mol), 160 mL ethylene glycol dimethylether and 50 mL water were added. After heating for 4 hours at 70° C., the reaction mixture was cooled on an ice bath. The solids were filtered and washed with a small amount of chloroform. The solids were suspended in 600 mL water, stirred for 30 minutes, and then filtered. This washing procedure was repeated with methanol. Following two crystallizations from trifluorotoluene using decolorizing charcoal, 5,5′-di(4-octyloxy-phenyl)-2,2′-bithiophene (Compound 4) was isolated as yellow/orange crystals (10.34 g, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07671083B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-a505cfd53a394aa78ab6c2bc3d5c9449
출처 메모uspto-grants-2010_03