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HRID 270012作成日:2026年10月25日

Sodium Carbonate → Benzaldehyde,2-benzo[b]thien-5-yl-

https://huagongshe.com/reaction/270012

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-Formylphenylboronic acidHCID 292189—
反応物5-Bromo-1-benzothiopheneHCID 2776578—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Benzaldehyde,2-benzo[b]thien-5-yl-HCID 6013976081%

反応条件

温度80 °C

反応手順

To a suspension of 5-Bromo-benzo[b]thiophene (compound PRE13) (3.68 g, 17.2 mmol) in toluene (183 mL) was added, under nitrogen, tetrakis(triphenylphosphine)-palladium (1.99 g, 1.72 mmol), then a solution of 2-formylphenylboronic acid (3.87 g, 25.8 mmol) in ethanol (20 mL) and at least dropwise aqueous sodium carbonate solution (3.64 g, 34.4 mmol) in water (20 mL). The reaction mixture was then heated to 80° C. for 3 h, cooled, concentrated, partitioned between ethyl acetate (120 mL) and water (70 mL) and acidified with hydrochloric acid (pH˜2). The organic layer was separated, dried over Na2SO4 and concentrated to give a crude residue that was purified by flash chromatography (silica, eluting solvent: (petroleum ether/AcOEt) 9.2/0.8) to give 3.31 g of compound PRE14 (orange yellow powder; yield=81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449481B2
出典データセットuspto-grants-2008_11
ORD IDord-7ee9c9f299ba4572b70062c261349b32
出典メモuspto-grants-2008_11