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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236561Generated: October 31, 2026

Piperidine → HCID 20216182, compound

https://huagongshe.com/reaction/236561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 20216188HCID 20216188—
ProductHCID 20216182HCID 20216182—

Reaction Steps

17.6 g. of α-ethyl-α-(4-fluorophenyl)-4-(2-bromoethoxy)-benzylalcohol and 30 ml. of dry piperidine are refluxed with stirring for two hours. Piperidine is distilled off from the reaction mixture under reduced pressure, to the residue water is added, and it is extracted with ether. The ethereal phase is washed to neutral with water, dried over anhydrous potassium carbonate, and then ether is distilled off. Crystallization of the residue from n-hexane yields 14.9 g. of the named compound, melting at 72° to 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04645774
Source datasetuspto-grants-1987_02
ORD IDord-63b42e631db2474b8a10cd283ed19534
Source noteuspto-grants-1987_02