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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102484Generated: October 31, 2026

HCID 16215260, compound → 790667-68-4

https://huagongshe.com/reaction/2102484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16215260HCID 16215260—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product790667-68-4HCID 5780319499.8%

Reaction Steps

A suspension of 4-(3-nitro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester (0.390 g) and 10% Pd/C (0.100 g) in ethanol was stirred under an hydrogen atmosphere (1 atm at balloon pressure) for 16 hr. The reaction mixture was filtered through a bed of Celite using ethyl acetate as solvent. Concentration afforded 4-(3-amino-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester as a clear oil (0.353 g, 90%). 1H NMR (400 MHz, DMSO-d6) δ 6.85 (t, 1H), 6.15-6.05 (m, 3H), 4.99 (br s, 2H), 4.43-4.30 (m, 1H), 3.67-3.53 (m, 2H), 3.20-3.06 (m, 2H), 1.89-1.80 (m, 2H), 1.53-1.4 (m, 2H), 1.38 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576085B2
Source datasetuspto-grants-2009_08
ORD IDord-3c51293c65c842a8881a331b4d25c319
Source noteuspto-grants-2009_08