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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104298Generated: October 31, 2026

p-Fluoronitrobenzene → 1,2,3,6-Tetrahydro-1-(4-nitrophenyl)-4-phenylpyridine

https://huagongshe.com/reaction/2104298

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2,3,6-Tetrahydro-4-phenylpyridineHCID 82553—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
Product1,2,3,6-Tetrahydro-1-(4-nitrophenyl)-4-phenylpyridineHCID 478103542%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 0.5 g (2.5 mmol) of 4-phenyl-1,2,3,6-tetrahydropyridine, 0.51 ml (2.8 mmol) of diisopropylethylamine, 0.71 g (5 mmol) of K2CO3, 0.40 g ((2.8 mmol) of 4-fluoronitrobenzene in 10 ml of DMF is heated at 100° C., for 24 hours. At the end of the reaction, the mixture is poured into 25 ml of a saturated solution of NaHCO3 and the product is extracted using 25 ml of AcOEt. After decantation, the organic solution is washed twice with 20 ml of water followed by 20 ml of brine, drying over magnesium sulphate, filtration and evaporation of the solvent under vacuum produce a yellow solid with a yield of 42%. Melting point: 185-192° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576241B2
Source datasetuspto-grants-2009_08
ORD IDord-98e0cf8450c14e52b78970e625611ce8
Source noteuspto-grants-2009_08