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HRID 330821作成日:2026年10月24日

Tributylamine → HCID 66691768、化合物

https://huagongshe.com/ja/reaction/330821

反応式

関与物質

役割名称HCID仕込み量
反応物TributylamineHCID 7622—
反応物Ethyl AcetateHCID 8857—
反応物3,3-Diethoxy-1-propeneHCID 62477—
反応物HCID 66691575HCID 66691575—
触媒Tetrabutylammonium ChlorideHCID 70681—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物HCID 66691768HCID 66691768—

反応条件

温度120 °C

反応手順

To 1.80 g (5.17 mmol) 1-ethoxy-4-((4-iodophenyl)ethynyl)benzene (XII.1) in 24 mL DMF are added 2.36 mL (15.5 mmol) 3,3-diethoxy-propene, 3.69 mL (15.5 mmol) tributylamine, 1.44 g (5.17 mmol) tetrabutylammoniumchloride and 0.04 g (0.16 mmol) palladium(II)acetate under argon. The mixture is stirred at 120° C. for 12 h. After that time, 1.18 mL (7.76 mmol) 3,3-diethoxy-propene are added and the mixture is stirred at 120° C. for 5 d. After cooling, EtOAc is added and the mixture is washed with 1N potassium hydrogensulfate solution and water. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; PE:DCM 1:1) to yield the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877754B2
出典データセットuspto-grants-2014_11
ORD IDord-caeaae0a8b5941e9b57e00af235f045f
出典メモuspto-grants-2014_11