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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242765생성일: 2026년 10월 26일

Sodium Hydroxide → 4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene

https://huagongshe.com/reaction/242765

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물(Benzo(1,2-b:4,5-b)dithiophene-4,8-dione)HCID 288478—
반응물n-Octyl p-ToluenesulfonateHCID 599296—
촉매ZincHCID 23994—
용매EthanolHCID 702—
생성물4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiopheneHCID 5828089962%

반응 단계

1.0 g (4.5 mmol) of benzo[1,2-b:4,5-b′]dithiophene-4,8-dione was mixed with 0.65 g (10 mmol) of zinc dust in a flask. Then, 4 ml of ethanol and 15 ml of 20% NaOH was added and the mixture was refluxed for 1 h. 4.3 mL octyl p-toluenesulfonate was added in portions with stirring until the color changed to red. The resulting precipitate was filtered, the filtrate was diluted with 100 mL water and extracted with 100 mL chloroform. The organic extraction was dried with anhydrous sodium sulfate and evaporated in vacuo. Column chromatography on silica gel using dichloromethane and hexanes mixed solvents yielded the pure title compound as a white solid (1.24 g, 62%). 1HNMR (CDCl3): δ0.88-0.91 (6H, t, J=7 Hz), 1.31-1.38 (16H, m), 1.54-1.58 (4H, m), 1.84-1.89 (4H, m), 4.26-4.29 (4H, J=7 Hz), 7.36-7.37 (2H, d, J=6 Hz), 7.47-7.48 (2H, d, J=6 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653228B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-e6513fd96e714cfd9160974fededf51d
출처 메모uspto-grants-2014_02