HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248569Generated: October 31, 2026
1-Phenylpiperidine → HCID 10064740, compound
https://huagongshe.com/reaction/2248569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperidine | HCID 20038 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10064740 | HCID 10064740 | 111.1% |
Reaction Steps
To a solution, cooled to between 0° C. and -5° C., comprising 8.46 g of sulphur trioxide in 45 cm3 of methylene chloride, there are added dropwise 9.3 g of dioxane followed by 17.1 g of N-phenylpiperidine dissolved in 45 cm3 of methylene chloride. The mixture is allowed to return to room temperature, then heated to reflux for 1 hour and evaporated to dryness, the residue is neutralized with 10% strength sodium carbonate solution, the aqueous phase is concentrated and the residue is dried and treated with 200 cm3 of phosphoryl chloride and 21.8 g of phosphorus pentachloride for 12 hours at room temperature. The mixture is evaporated to dryness, the residue is taken up in chloroform with a little water, the organic phase is separated, dried over sodium sulphate and filtered and the solvent is evaporated off. 19 g of expected product are obtained, which product is used as it is in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05041436 |
|---|
| Source dataset | uspto-grants-1991_08 |
|---|
| ORD ID | ord-b2d613a171d3434b8b1f570f4c1fc72f |
|---|
| Source note | uspto-grants-1991_08 |
|---|