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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452779Generated: October 30, 2026

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

https://huagongshe.com/reaction/1452779

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 mmole) of 4-phenyl-1,2,3,6-tetrahydropyridine, 0.51 ml (2.8 mmole) of diisopropylethylamine, 0.71 g (5 mmole) of K2CO3, 0.40 g ((2.8 mmole) 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 numberUS07473779B2
Source datasetuspto-grants-2009_01
ORD IDord-3438d1070b8c492aa63396454fd34f3e
Source noteuspto-grants-2009_01