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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248569Generated: October 31, 2026

1-Phenylpiperidine → HCID 10064740, compound

https://huagongshe.com/reaction/2248569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperidineHCID 20038—
ReactantSulfur trioxideHCID 24682—
Reactant1,4-DioxaneHCID 31275—
SolventDichloromethaneHCID 6344—
ProductHCID 10064740HCID 10064740111.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041436
Source datasetuspto-grants-1991_08
ORD IDord-b2d613a171d3434b8b1f570f4c1fc72f
Source noteuspto-grants-1991_08