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HRID 242765作成日:2026年10月26日

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

https://huagongshe.com/reaction/242765

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物(Benzo(1,2-b:4,5-b)dithiophene-4,8-dione)HCID 288478—
反応物n-Octyl p-ToluenesulfonateHCID 599296—
触媒ZincHCID 23994—
溶媒EthanolHCID 702—
生成物4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiopheneHCID 5828089962%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653228B2
出典データセットuspto-grants-2014_02
ORD IDord-e6513fd96e714cfd9160974fededf51d
出典メモuspto-grants-2014_02