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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347385Generated: October 29, 2026

Water → 5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehyde

https://huagongshe.com/reaction/347385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantN-[2-(5-formyl-2,4-dimethoxyphenylethynyl)phenyl]acetamideHCID 11438686—
CatalystPalladium ChlorideHCID 24290—
SolventEthyl AcetateHCID 8857—
Product5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehydeHCID 2108253040.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-[2-(5-Formyl-2,4-dimethoxy-phenyl ethynyl)phenyl]acetamide (Ex-57E, 535 mg, 1.6 mmol) was added to 150 mL of DMF (nitrogen purged) at room temperature and the resulting solution was heated to 80° C. Palladium(II) chloride (22 mg) was added in one portion. After 6 h the reaction mixture was poured into water (50 mL) and EtOAc (50 mL), and the layers were cut. The organic layer was filtered through Celite, washed with brine, and concentrated to an orange solid. The crude was purified by silica gel chromatography (25% ethyl acetate/hexane) to yield 210 mg (39%) of 5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehyde as a white solid. 1H-NMR (300 MHz, DMSO-d6) 10.22 (s, 1H), 8.13 (d, 1H, J=8.1 Hz), 7.71 (s, 1H), 7.55 (d, 1H, J=6.3 Hz), 7.25 (m, 2H, J=6.9 Hz), 6.84 (s, 1H), 6.64 (s, 1H), 4.01 (s, 3H), 3.87 (s, 3H), 2.13 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-1694fb05fc7d4adeb6d8af77eb19a6be
Source noteuspto-grants-2007_02