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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22938Generated: October 29, 2026

p-Fluoronitrobenzene → HCID 178511611, compound

https://huagongshe.com/reaction/22938

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178511674HCID 178511674—
SolventDimethylacetamideHCID 31374—
ProductHCID 178511611HCID 17851161182%

Reaction Conditions

Temperature144 °C

Reaction Steps

A N,N-dimethylacetamide (30 ml) solution containing 4-nitrofluorobenzene (1.69 g) and trans-1,4-cyclohexanediamine (4.1 g) was stirred at 144° C. for 3 days. After cooling, an aqueous saturated potassium carbonate solution was added to the reaction solution, and the reaction mixture was extracted with ethyl acetate. The extract was dried over anhydrous potassium carbonate, and then, the solvent was removed under reduced pressure. The residue was purified by silica gel flash column chromatography (solvent: chloroform-methanol-ammonia (90:10:1)), and the solvent was removed to obtain trans-N-(4-nitrophenyl)-1,4-cyclohexanediamine (Reference Example 3-41 in Table 5) (2.31 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849622B2
Source datasetuspto-grants-2005_02
ORD IDord-a63b99af0ecf4446926d9168dae24558
Source noteuspto-grants-2005_02