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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2060346생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2060346

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물NitrogenHCID 947—
반응물Methyl 2-(5-bromothiophen-2-yl)acetateHCID 12403315—
반응물2-Aminophenylboronic acid hydrochlorideHCID 16427090—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물[5-(2-Amino-phenyl)-thiophen-2-yl]-acetic acid methyl esterHCID 1611616051.3%

반응 조건

온도100 °C

반응 단계

(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, 3H); 3.83 (s, 2H); 3.92-4.07 (br.s, 2H); 6.74 (d, 1H); 6.76 (td, 1H, J1=7.6 Hz, J2=1.3 Hz); 6.92 (d, 1H, J=3.5 Hz); 7.02 (d, 1H, J=3.5 Hz); 7.11 (td, 1H, J1=7.6 Hz, J2=1.5 Hz); 7.23 (dd, 14H, J1=7.6 Hz, J2=1.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08278356B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-8c0783c11b7b459eb402ec7f9cc21960
출처 메모uspto-grants-2012_10