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HRID 1944261作成日:2026年10月25日

Ethanol → (2'-Amino-biphenyl-3-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/1944261

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(2-Aminophenyl)boronic acidHCID 2773216—
反応物Methyl 2-(3-bromophenyl)acetateHCID 11746402—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TolueneHCID 1140—
生成物(2'-Amino-biphenyl-3-yl)-acetic acid methyl esterHCID 16116037106.8%

反応条件

温度100 °C

反応手順

(The following reaction is done in an oxygenfree N2 atmosphere.) Add ethanol (0.8 mL), Tetrakis-(triphenylphosphine)-palladium(0) (30 mg, 2.2 mol %) and Na2CO3 decahydrate (944 mg, 3.30 mmol; presolved in 1.2 mL H2O) subsequently to dissolved 2-Amino-benzeneboronic acid (48) (201 mg, 1.30 mmol) in toluene (6.0 mL). Degas the reaction mixture for 5 times and flood with N2 again. Add (3-Bromo-phenyl)-acetic acid methyl ester (47) (270 mg, 1.18 mmol) in toluene (6.0 mL), degas again (5 times) and stir the reaction solution overnight at 100° C. Partition the reaction solution between EtOAc and brine (1+1) and extract the separated aqueous layer 3 times with EtOAc. Wash combined organic layer with brine and dry with Na2SO4. Remove solvent under reduced pressure and purify the crude product by preparative radial chromatography (silica gel 60PF, CyH/EtOAc 3+1) to obtain (2′-Amino-biphenyl-3-yl)-acetic acid methyl ester (49) as an orange oil (304 mg, 81%). 1H NMR (400 MHz, CDCl3): 3.66 (s, 2H); 3.69 (s, 3H); 3.62-3.86 (br.s, 2H); 6.75 (d, 1H, J=8.1 Hz); 6.80 (t, 1H, J=7.3 Hz); 7.11 (d, 1H, J=7.3 Hz); 7.15 (d, 1H, J=8.1 Hz); 7.22-7.26 (br.m, 1H); 7.32-7.42 (m, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394835B2
出典データセットuspto-grants-2013_03
ORD IDord-20d22edd56d8473abd3812d8751ed192
出典メモuspto-grants-2013_03