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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075004생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2075004

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, 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07919532B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-c8e007133a6b4f87919f3eb0ff66e439
출처 메모uspto-grants-2011_04