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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909357Generated: October 31, 2026

Ammonium formate → 4-Benzo[1,3]dioxol-4-yl-piperidine

https://huagongshe.com/reaction/1909357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4-(Benzo[1,3]dioxol-4-yl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 70656446—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Benzo[1,3]dioxol-4-yl-piperidineHCID 70657290100%

Reaction Steps

Pd/C 10% (169 mg, 159 μmol,) was added to a solution of 4-(benzo[1,3]dioxol-4-yl)-1,2,3,6-tetrahydropyridine hydrochloride (760 mg, 3.17 mmol) and ammonium formate (1.00 g, 15.9 mmol) in methanol (28.8 ml) under argon. After refluxing for 60 min the reaction mixture was cooled to room temperature, filtrated and concentrated under reduced pressure. Saturated sodium bicarbonate solution was added to the residue and the mixture was extracted with dichloromethane (3×25 mL). The organic layers were dried over MgSO4 and concentrated in vacuo to yield the title compound as a white solid (0.654 grs, 100%). MS (ISP) m/z=206.0[(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598357B2
Source datasetuspto-grants-2013_12
ORD IDord-ae532a8722ee49fe9ab6be0c258bebc9
Source noteuspto-grants-2013_12