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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399303Generated: October 26, 2026

Piperidine → 1-(Naphthalen-2-yl)piperidine

https://huagongshe.com/reaction/399303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-Naphthyl TrifluoromethanesulfonateHCID 4546341—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 178506046HCID 178506046—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
Product1-(Naphthalen-2-yl)piperidineHCID 23070977%

Reaction Conditions

Temperature105 °C

Reaction Steps

The method described in this example is representative of method "A". Into a screw-capped test tube were weighed 8.6 mg (0.015 mmol) Pd(dba)2, 12.8 mg (0.023 mmol) DPPF, and 44.3 mg (0.462 mmol) sodium t-butoxide (NaO-t-Bu). The solid materials were suspended in 8 ml of toluene. 2-Naphthyltriflate (85.0 mg, 0.308 mmol) was dissolved in 1 ml of toluene and added to the test tube. The test tube was sealed with a cap containing a polytetrafluoroethylene (PTFE) septum and removed from the dry box. Piperidine (40.0 μl, 0.462 mmol) was added to the test tube by syringe. The reaction mixture was heated at 105° C. for 5 hours. Thin layer chromatography (TLC) of the reaction mixture indicated complete consumption of the naphthyltriflate. The reaction mixture was cooled to room temperature, and the volatile materials were removed by rotary evaporation. Sublimation (120° C., 0.1 torr) of the resulting residue afforded N-(2-naphthyl)piperidine as a white solid (50.0 mg, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817877
Source datasetuspto-grants-1998_10
ORD IDord-e8569e87b83f41cf84c4832f320de4b8
Source noteuspto-grants-1998_10