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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483953Generated: October 31, 2026

(R)-tert-butyl-2-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylate → (R)-tert-butyl-2-((3-amino-2-cyanophenoxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1483953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-butyl-2-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylateHCID 86714287—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(R)-tert-butyl-2-((3-amino-2-cyanophenoxy)methyl)piperidine-1-carboxylateHCID 8671428688%

Reaction Steps

To a solution of (R)-tert-butyl-2-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylate (Example 15e, 10.8 g, 29.85 mmol) in ethyl acetate (86 mL) was added 10% Pd/C (1.08 g, 3 mmol). H2 was added by balloon, and the mixture was stirred for 48 hours at room temperature. Upon completion, the mixture was filtered through a pad of celite, and the solvent was removed in vacuo. The residue was recrystallized from ethyl acetate/hexanes to afford (R)-tert-butyl-2-((3-amino-2-cyanophenoxy)methyl)piperidine-1-carboxylate (8.65 g, 88%) as an off white solid. MS 323 (MH+-boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09420814B2
Source datasetuspto-grants-2016_08
ORD IDord-0bfef514fa5c4e13bf8cbf1137eebaa3
Source noteuspto-grants-2016_08