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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1256689Erstellt: 26. Oktober 2026

Nitrogen → [5-(3-Nitro-phenyl)-thiophen-2-yl]acetic acid methyl ester

https://huagongshe.com/reaction/1256689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
Edukt3-Nitrophenylboronic AcidHCID 1677—
EduktSodium CarbonateHCID 10340—
EduktMethyl 2-(5-bromothiophen-2-yl)acetateHCID 12403315—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt[5-(3-Nitro-phenyl)-thiophen-2-yl]acetic acid methyl esterHCID 5978679058,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

FR544 (The following reaction is carried out in an N2 atmosphere.) Dissolve Tetrakis-(triphenylphosphine)-palladium(0) (1.12 g, 0.97 mmol) and ester (43) (4.57 g, 19.44 mmol) in toluene (200 mL) and EtOH (20.0 mL), degas the reaction mixture carefully (5 times) and flush with N2. Add 3-nitrophenylboronic acid (3.57 g, 21.38 mmol) and a 3 M aqueous Na2CO3 solution (18.1 mL, 54.3 mmol), degas the reaction mixture again carefully (5 times) and flush with N2. Stir the mixture for 18 h at 100° C. Partition the reaction solution between EtOAc and water and extract the separated aqueous layer with EtOAc (3 times). Wash combined organic layer with brine and dry it with Na2SO4. Purify the obtained crude product by preparative radial chromatography (silica gel, EtOAc/CyH 1+5) to obtain [5-(3-nitro-phenyl)-thiophen-2-yl]acetic acid methyl ester (56) as a yellow solid (3.15 g, 58%). 1H NMR (400 MHz, CDCl3): 3.75 (s, 3H); 3.85 (s, 2H); 6.94 (br.d, 1H, J=3.8 Hz); 7.27 (d, 1H, J=3.8 Hz); 7.51 (t, 1H, J=8.0 Hz); 7.84 (ddd, 1H, J1=7.8 Hz, J2=1.5 Hz, J3=0.8 Hz); 8.08 (ddd, 1H, J1=8.3 Hz, J2=2.1 Hz, J3=1.0 Hz); 8.39 (t, 1H, J=1.9 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08461207B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-0652c2030faf4ce181f454d758323aba
Quellennotizuspto-grants-2013_06