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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551007Generated: October 28, 2026

Ethyl Oxo(Piperidin-1-Yl)Acetate → ethyl 2-(4-nitro-1H-indol-3-yl)-2-oxoacetate

https://huagongshe.com/reaction/551007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl Oxo(Piperidin-1-Yl)AcetateHCID 104406—
Reactant4-Nitro-1H-indoleHCID 145766—
ReactantDiphosphoryl tetrachlorideHCID 4432411—
Productethyl 2-(4-nitro-1H-indol-3-yl)-2-oxoacetateHCID 14131875—

Reaction Steps

Diphosphoryl chloride (23.5 mL, 170 mmol) was added dropwise to a stirred mixture of 4-nitroindole (25.0 g, 154 mmol) and ethyl 1-piperidineglyoxylate (29.0 g, 170 mmol) at 0° C. The mixture was allowed to warm slowly to ambient temperature and stirring was continued for 18 h. The reaction mixture was cooled to 0° C. and quenched carefully by addition of EtOH (50 mL), followed by saturated aqueous NaHCO3 until no further effervescence was observed. The precipitated yellow solid was isolated by filtration, washed with H2O, and dried in vacuo to give the title compound. MS: m/z=263 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947677B2
Source datasetuspto-grants-2011_05
ORD IDord-92830f1cdf3b41fe93642a6f6b0eca62
Source noteuspto-grants-2011_05