HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine → 1-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine | HCID 11128034 | — |
| Reactant | p-Nitrophenyl 3-pyridylacetate | HCID 20280550 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine | HCID 20280532 | 52.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04521428 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-f7a8c886b30c4963a05c64b547a0290b |
| Source note | uspto-grants-1985_06 |