HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902676Generated: November 1, 2026
Potassium Iodide → N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butenedioate
https://huagongshe.com/reaction/1902676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-(N,N-diphenylamino)-1-chloropropane | HCID 10658053 | — |
| Reactant | 4-(3-Methylphenyl)piperidine hydrochloride | HCID 21936967 | — |
| Reactant | N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butanedioate | HCID 86738711 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butenedioate | HCID 70530333 | — |
Reaction Steps
A mixture of 7.37 g. (0.030 moles) of 3-[N,N-diphenylamino]-1-chloropropane, 6.0 g. (0.024 moles) of 4-(3-methylphenyl)-piperidine hydrochloride, 3.92 g. (0.024 moles) of potassium iodide, and 5.30 g. (0.050 moles) of sodium carbonate in 60 ml. of n-butanol is refluxed for about 16 hours. Solvent is evaporated and the residue is dissolved in chloroform and washed with water. The chloroform solution is dried and passed through a column of silica gel. The product is eluted with acetonitrile. The product fractions are combined, concentrated, and converted to the maleate salt in ether. The resulting crystals recrystallized from acetonitrile to give 7.2 g. of N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butanedioate (1:1), mp. 137.5°-139.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04364954 |
|---|
| Source dataset | uspto-grants-1982_12 |
|---|
| ORD ID | ord-e51816231e014e4ea3646c46d7142062 |
|---|
| Source note | uspto-grants-1982_12 |
|---|