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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268780Generated: October 31, 2026

(3-Chlorophenyl)boronic acid → HCID 59831833, compound

https://huagongshe.com/reaction/268780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
ReactantHCID 54059723HCID 54059723—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59831833HCID 5983183362%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 3-(1H-indol-6-yl)-acrylic acid methyl ester XXX (0.4 g, 2.0 mmol), 3-chlorophenyl boronic acid (0.62 g, 4.0 mmol), [RhCl(cod)]2 (49 mg, 0.10 mmol) and TEA (0.42 ml, 3.0 mmol) in water (6 ml) and 1,4-dioxane (1 ml) was stirred at 95° C. for 18 hours. The reaction mixture was cooled to room temperature, and partitioned between H2O and EtOAc. The aqueous layer was extracted with EtOAc. The organic layers were combined, dried over MgSO4, filtered, concentrated, and purified via flash chromatography (hexane/EtOAc) to provide 3-(1H-indol-6-yl)-3-(3-chloro-phenyl)-propionic acid methyl ester XL (90 mg, 62% yield) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446118B2
Source datasetuspto-grants-2008_11
ORD IDord-514bce0ce6094f258bffd68a1234e166
Source noteuspto-grants-2008_11