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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195656Generated: October 29, 2026

Dimethylformamide → 1-(4-Methyl-2-nitrophenyl)piperidine

https://huagongshe.com/reaction/2195656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Chloro-3-nitrotolueneHCID 6976—
ReactantPiperidineHCID 8082—
SolventWaterHCID 962—
Product1-(4-Methyl-2-nitrophenyl)piperidineHCID 1279821746.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Piperidine (660 μl, 6.66 mmol, commercially available product) was added at room temperature to an N,N-dimethylformamide (DMF; 1 ml) solution of 4-chloro-3-nitrotoluene (358 mg, 2.08 mmol, commercially available product). The resulting mixture was stirred at 100° C. for 17 hours. The mixture was cooled to room temperature, and then water was added thereto. The resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (50 g, hexane/ethyl acetate=50/1). Thus, 1-(4-methyl-2-nitrophenyl)piperidine (212 mg, 46.2%) was yielded as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338362B2
Source datasetuspto-grants-2012_12
ORD IDord-1169033a61c144048fed6a30570c69c5
Source noteuspto-grants-2012_12