Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075004Generated: October 26, 2026

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

https://huagongshe.com/reaction/2075004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantNitrogenHCID 947—
ReactantMethyl 2-(5-bromothiophen-2-yl)acetateHCID 12403315—
Reactant2-Aminophenylboronic acid hydrochlorideHCID 16427090—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product[5-(2-Amino-phenyl)-thiophen-2-yl]-acetic acid methyl esterHCID 1611616051.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

(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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919532B2
Source datasetuspto-grants-2011_04
ORD IDord-c8e007133a6b4f87919f3eb0ff66e439
Source noteuspto-grants-2011_04