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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531176Generated: October 31, 2026

2-Chloro-1-fluoro-4-nitrobenzene → (2-Chloro-4-nitro-phenyl)-methyl(1-methyl-pyrrolidin-3-yl)-amine

https://huagongshe.com/reaction/1531176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
ReactantN,1-dimethylpyrrolidin-3-amineHCID 2758520—
SolventEthyl AcetateHCID 8857—
Product(2-Chloro-4-nitro-phenyl)-methyl(1-methyl-pyrrolidin-3-yl)-amineHCID 18543297—

Reaction Steps

3-Chloro-4-fluoronitrobenzene (1.0 g) and N,N′-dimethyl-3-aminopyrrolidine (1.72 g) are combined and stirred for approximately 24 hours. The mixture is then diluted with ethyl acetate, washed twice with water and once with saturated sodium chloride, and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the residue is chromatographed over silica gel (pure ethyl acetate followed by pure methanol is used as the eluants) to provide the desired product as a yellow oil. p Using the above procedure and appropriate starting materials the following compounds were prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197803B1
Source datasetuspto-grants-2001_03
ORD IDord-13e9fd38157a4a72981f019a1fc1de62
Source noteuspto-grants-2001_03