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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864770Generated: October 27, 2026

Water → 3-(1H-indol-5-yl)benzaldehyde

https://huagongshe.com/reaction/1864770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactant5-BromoindoleHCID 24905—
Reactant3-Formylphenylboronic acidHCID 2734356—
Solvent1,4-DioxaneHCID 31275—
Product3-(1H-indol-5-yl)benzaldehydeHCID 413587957%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-indole (8.7 g, 44.4 mmol), 3-formylbenzeneboronic acid (10 g, 66.7 mmol), cesium carbonate in water (2M, 88.8 mL, 178 mmol) in 450 mL of dioxane was degassed (evacuate in vacuo and pressurize with nitrogen, 3 times) PdCl2(dppf).DCM (1.1 g, 1.3 mmol) was added and the mixture degassed one more time as described above. The resulting mixture was heated at 100° C. for 3 h, then it was allowed to cool to room temperature and partitioned between diethyl ether and water. The aqueous phase was extracted with diethyl ether and the combined organic phases were washed with water, brine, dried over MgSO4, filtered and evaporated to give the crude product. Chromatography on silica gel (elution with ethyl acetate/heptane) afforded 5.6 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625889B2
Source datasetuspto-grants-2009_12
ORD IDord-168053c28ba84e3c8056cba3d19a2d6c
Source noteuspto-grants-2009_12