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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435556Generated: October 27, 2026

Water → 3-(1H-indol-5-yl)benzaldehyde

https://huagongshe.com/reaction/1435556

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 numberUS07618650B2
Source datasetuspto-grants-2009_11
ORD IDord-74975e79ff8344c088816e1c27e1b5e0
Source noteuspto-grants-2009_11