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HRID 884068作成日:2026年10月25日

Potassium Carbonate → (E)-ethyl 2-(4-(methoxymethoxy)phenyl)-3-o-tolylpent-2-enoate

https://huagongshe.com/reaction/884068

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Ethyl pent-2-yn-1-oateHCID 99169—
反応物2-Methylphenyl boronic acidHCID 2733267—
反応物1-Iodo-4-(methoxymethoxy)benzeneHCID 11032730—
触媒Bis(benzonitrile)palladium chlorideHCID 498840—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(E)-ethyl 2-(4-(methoxymethoxy)phenyl)-3-o-tolylpent-2-enoateHCID 8663029427%

反応手順

A mixture of Ethyl 2-pentynoate (350 mg, 2.77 mmol), 1-iodo-4-(methoxymethoxy)benzene (1.46 g, 5.53 mmol), 2-Methylphenylboronic acid (753 mg, 5.53 mmol) and K2CO3 (766 mg, 5.54 mmol) in DMF (8.5 ml)-H2O (2.2 ml) was stirred at room temperature for 10 min. Then PdCl2(PhCN)2 (10.6 mg, 0.0276 mmol) was added under Ar atmosphere, and the mixture was stirred at room temperature for 24 h. The reaction was quenched with H2O under ice cooling, and the whole was extracted with Et2O. The organic layer was washed with H2O, brine, dried over Na2SO4, then concentrated. Purification by silica gel flash column chromatography (eluent: hexane/AcOEt, 30:1) gave 2a (27%). 2a: colorless oil; 1H-NMR (CDCl3) δ 1.02 (3H, t, J=7.5 Hz), 1.33 (3H, t, J=7.1 Hz), 2.04 (3H, s), 2.56 (2H, m), 3.42 (3H, s), 4.30 (2H, m), 5.06 (2H, s), 6.72 (2H, d, J=8.8 Hz), 6.88 (2H, d, J=8.8 Hz), 7.00-7.12 (5H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236987B2
出典データセットuspto-grants-2012_08
ORD IDord-73d9815309334c659f434151f4e29d34
出典メモuspto-grants-2012_08