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HRID 2075004作成日:2026年10月27日

Ethanol → [5-(2-Amino-phenyl)-thiophen-2-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/2075004

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物NitrogenHCID 947—
反応物Methyl 2-(5-bromothiophen-2-yl)acetateHCID 12403315—
反応物2-Aminophenylboronic acid hydrochlorideHCID 16427090—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物[5-(2-Amino-phenyl)-thiophen-2-yl]-acetic acid methyl esterHCID 1611616051.3%

反応条件

温度100 °C

反応手順

(The following reaction is carried out in an N2 atmosphere.) Ethanol (3.7 mL), tetrakis-(triphenylphosphine)-palladium(0) (289 mg, 0.25 mmol) and Na2CO3 decahydrate (4.0 g, 14.0 mmol) dissolved in water (5.2 mL) are subsequently added to a solution of 2-amino-benzeneboronic acid hydrochloride (910 mg, 5.25 mmol) in toluene (52 mL). Degas the reaction mixture carefully (5 times) and flush with N2 again. A solution of (5-bromo-thiophen-2-yl)-acetic acid methyl ester (43) (1.17 g, 5.0 mmol) in toluene (4.5 mL) is added. Degas the mixture again (5 times) and stir for 22 h at 100° C. Partition the reaction solution between EtOAc and brine and extract the separated aqueous layer with EtOAc (3 times). Wash combined organic layer with water and brine and dry it with Na2SO4. Purify the crude product by preparative radial chromatography (CyH/EtOAc 5+1] to obtain [5-(2-amino-phenyl)-thiophen-2-yl]-acetic acid methyl ester (44) as a brown oil (634 mg, 51%). 1H NMR (400 MHz, CDCl3): 3.73 (s, 3 H); 3.83 (s, 2 H); 3.92-4.07 (br.s, 2 H); 6.74 (d, 1 H); 6.76 (td, 1 H, J1=7.6 Hz, J2=1.3 Hz); 6.92 (d, 1 H, J=3.5 Hz); 7.02 (d, 1 H, J=3.5 Hz); 7.11 (td, 1 H, J=7.6 Hz, J2=1.5 Hz); 7.23 (dd, 14 H, J1=7.6 Hz, J2=1.5 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07919532B2
出典データセットuspto-grants-2011_04
ORD IDord-c8e007133a6b4f87919f3eb0ff66e439
出典メモuspto-grants-2011_04