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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633431Generated: October 31, 2026

Tert-butyl 4-(2-(difluoromethoxy)-4-nitrophenoxy)piperidine-1-carboxylate → Tert-butyl 4-(4-amino-2-(difluoromethoxy)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/633431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-(difluoromethoxy)-4-nitrophenoxy)piperidine-1-carboxylateHCID 86704525—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(4-amino-2-(difluoromethoxy)phenoxy)piperidine-1-carboxylateHCID 8670452663.1%

Reaction Steps

The general hydrogenation procedure as described herein was used with tert-butyl 4-(2-(difluoromethoxy)-4-nitrophenoxy)piperidine-1-carboxylate (193 mg, 0.5 mmol), palladium on charcoal (39 mg) and MeOH (5 mL) under atmospheric pressure (H2 balloon) to give the product (113 mg, 63% yield) after purification by column chromatography on silica gel using EtOAc/heptane (2:8 to 6:4) as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-3d8b908a75a7409495981f94d1a99f33
Source noteuspto-grants-2016_04