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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270974Generated: October 30, 2026

Diethyl Oxalate → HCID 178473094, compound

https://huagongshe.com/reaction/2270974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant1-(5-chloro-1H-indol-3-yl)ethanoneHCID 2762971—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 178473094HCID 17847309481%

Reaction Steps

In 100 ml of EtOH was dissolved 2.99 g (126 mmol) of sodium under heating. The EtOH was evaporated under reduced pressure and the residue was suspended in THF (200 ml). The THF was evaporated. To the suspension of the residue in THF (124 ml) was added 18.1 g (124 mmol) of diethyl oxalate. Subsequently, to the above suspension was added at room temperature, 12 g (62 mmol) of 3-acetyl-5-chloroindole. After stirring for 3 hours, the mixture was stirred at 50° C. for additional 16 hours. The solvent was removed under reduced pressure. The resulting residue was washed with ether, and added to 1N hydrochloric acid (120 ml). The precipitated crystal was collected by filtration, and washed with water and ethyl acetate. Then the crystal was purified by recrystallization from dioxane and dried at 80° C. under reduced pressure to give 14.7 g of the titled compound. Yield: 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333323B1
Source datasetuspto-grants-2001_12
ORD IDord-024924a6aee34219b208986b2ee0317b
Source noteuspto-grants-2001_12