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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064058Generated: November 3, 2026

Sodium Carbonate → HCID 57423906, compound

https://huagongshe.com/reaction/2064058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystPotassium IodideHCID 4875—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57423906HCID 5742390684%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethyl-4-amino-1-piperidine-carboxylate (18.3 g, 106 mmol) was added to a stirred suspension of 3-fluoro-4-nitrotoluene (15.0 g, 97 mmol), sodium carbonate (10.3 g, 97 mmol) and potassium iodide (0.16 g, 0.97 mmol) in dimethylformamide (150 mL). The mixture was heated to 50° C., stirred for 15 hours and then allowed to cool. The reaction mixture was diluted with water (200 mL) and ethyl acetate (200 mL). The organic phase was separated and the aqueous phase was extracted with ethyl acetate (2×200 mL). The organic extracts were combined, extracted with a 10% aqueous solution of citric acid (250 mL), dried over MgSO4 and evaporated under reduced pressure. The residue was purified by column chromatography on silica, eluting with dichloromethane and then ethyl acetate/hexane (7:8) to give the title compound (25.0 g, 84% yield) as a yellow solid. (Rf: 0.3 (ethyl acetate/hexane 7:8))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288413B2
Source datasetuspto-grants-2012_10
ORD IDord-15f70ff8de18495bad1e467ca0bce737
Source noteuspto-grants-2012_10