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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609691Generated: October 30, 2026

N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine → 4-(4,5,6,7-Tetrafluoroindol-3-yl)piperidine

https://huagongshe.com/reaction/609691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidineHCID 11395638—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
Product4-(4,5,6,7-Tetrafluoroindol-3-yl)piperidineHCID 2261558590%

Reaction Steps

To a solution of N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine (20.0 g, 49.21 mmol) [prepared as described in Step 1 above] in argon deoxygenated 80% ethanol/tetrahydrofuran (800 ml) was added 10% Pd-C (5 g), and the resulting mixture was stirred under a hydrogen atmosphere (1 atm) for 3 h. The mixture was degassed under argon, filtered through Celite, and concentrated in vacuo. The solid residue was recrystallized from methylene chloride/hexane to afford 4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine (90%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-e7423c88d07a4634bafb2a34980e7ae6
Source noteuspto-grants-1999_12