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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935281Generated: October 25, 2026

Sodium Carbonate → 3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl ester

https://huagongshe.com/reaction/1935281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Indolylboronic acidHCID 2734361—
Reactant3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl esterHCID 67483447—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl esterHCID 6748521836%

Reaction Conditions

Temperature25 °C

Reaction Steps

A slurry of dichlorobis(triphenylphosphine)palladium(II) (119 mg, 0.17 mmol) in 1,2-dimethoxyethane (10 mL) was treated with 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (1.00 g, 2.79 mmol). The reaction slurry was stirred at 25° C. for 10 min and then treated with a mixture of 5-indolylboronic acid (670 mg, 4.19 mmol) in water (5 mL) and a 2M aqueous sodium carbonate solution (2.8 mL, 5.58 mmol). The resulting reaction mixture was heated under reflux for 2 h. The reaction mixture was allowed to cool to 25° C. and then filtered to remove the catalyst. The filtrate was partitioned between water (50 mL) and methylene chloride (50 mL), and the layers were separated. The aqueous layer was further extracted with methylene chloride (50 mL). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/2 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-[4-(1H-indol-5-yl)-phenyl]-propionic acid methyl ester (347 mg, 36%) as a light brown oil: EI-HRMS m/e calcd for C23H25NO2 (M+) 347.1885, found 347.1887.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384220B2
Source datasetuspto-grants-2002_05
ORD IDord-f5236949d3e94226b4c867a223d4a7c3
Source noteuspto-grants-2002_05