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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064050Generated: October 26, 2026

Sodium Carbonate → 1-Carbethoxy-4-(5-chloro-2-nitroanilino)-piperidine

https://huagongshe.com/reaction/2064050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,4-DichloronitrobenzeneHCID 11899—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
CatalystPotassium IodideHCID 4875—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Carbethoxy-4-(5-chloro-2-nitroanilino)-piperidineHCID 1379216665%

Reaction Conditions

Temperature140 °C

Reaction Steps

Ethyl-4-amino-1-piperidine-carboxylate (29.6 g, 0.17 mol) was added to a stirred suspension of 2,4-dichloronitrobenzene (30.0 g, 0.16 mol), sodium carbonate (16.5 g, 0.16 mol) and potassium iodide (0.26 g, 0.0016 mol) in dimethylformamide (300 mL). The mixture was heated to 140° C., stirred for 15 hours and then allowed to cool. The reaction mixture was diluted with water (400 mL) and ethyl acetate (600 mL). The aqueous phase was separated and the organic phase was extracted with water (2×300 mL). The organic phase was dried over MgSO4 and evaporated under reduced pressure. The residue was purified by column chromatography on silica, eluting with ethyl acetate/hexane (1:3) to give the title compound (33.0 g, 65% yield) as an orange solid. (Rf: 0.4 (ethyl acetate/hexane 1:3))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288413B2
Source datasetuspto-grants-2012_10
ORD IDord-9da7fe6bd19140d5af0eef0809b165df
Source noteuspto-grants-2012_10