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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248014Generated: October 26, 2026

4-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine → 1-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/1248014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridineHCID 11128034—
Reactantp-Nitrophenyl 3-pyridylacetateHCID 20280550—
SolventEthanolHCID 702—
Product1-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridineHCID 2028053252.8%

Reaction Steps

A suspension of 11.3 g of p-nitrophenyl 3-pyridylacetate and 10 g of 4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine in 150 ml of ethanol is stirred 1 hour at room temperature, then concentrated under reduced pressure. The residue is dissolved in diethyl ether, the solution is washed with water, then with sodium hydroxide and again with water, dried on anhydrous sodium sulfate and concentrated. Thus, 1-(3-pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine (8 g) is obtained as an oil which is used for the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04521428
Source datasetuspto-grants-1985_06
ORD IDord-f7a8c886b30c4963a05c64b547a0290b
Source noteuspto-grants-1985_06