HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3,6-Tetrahydro-4-phenylpyridine → HCID 53925922, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3,6-Tetrahydro-4-phenylpyridine | HCID 82553 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(1-Hydroxy-3-chloropropyl)-3,4-dihydrocarbostyril | HCID 20229459 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53925922 | HCID 53925922 | — |
Reaction Steps
2.5 Grams of 6-[1-hydroxy-3-chloropropyl]-3,4-dihydrocarbostyril and 3.0 g of 4-phenyl-1,2,5,6-tetrahydropyridine were mixed in 50 ml of toluene and the mixture was refluxed by heating for 5 hours, then toluene was removed by distillation. To the residue thus obtained was added 50 ml of 5%-sodium hydrogencarbonate aqueous solution and was extracted with chloroform. The chloroform layer was washed with water and dried, then chloroform was removed by distillation. The residue thus obtained was recrystallized from ethanol to obtain 2.1 of 6-[3-(4-phenyl-1,2,5,6-tetrahydropyridyl)-1-propenyl]-3,4-dihydrocarbostyril in light yellow plate-like crystals. Melting point: 182°-183° C. (decomposed).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04455422 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-1ca000429a964c1c95d5c8f834764e2b |
| Source note | uspto-grants-1984_06 |