Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524932Generated: October 27, 2026

Sodium hydride → HCID 86720990, compound

https://huagongshe.com/reaction/524932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl (3S)-3-hydroxypiperidine-1-carboxylateHCID 1514399—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86720990HCID 8672099087%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (492.0 mg, 12.30 mmol) was added to a solution of tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate (2.095 g, 10.41 mmol) in THF (20 mL) and the reaction stirred at 0° C. for 15 minutes. A suspension of 4-chloro-3-nitro-pyridine (1.5 g, 9.461 mmol) in THF (10 mL) was added and the reaction allowed to warm slowly to ambient temperature over 2 hours. The reaction was quenched with water and the mixture was partitioned between EtOAc and brine. The combined organic extract was washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 80 g column, eluting with 0 to 100% EtOAc/Petroleum Ether) to give tert-butyl (3S)-3-[(3-nitro-4-pyridyl)oxy]piperidine-1-carboxylate as a pale yellow solid (2.65 g, 87% Yield, 93% ee). MS (ES+) 324.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-4780ed625eb8453e9e6b6fbefcaac2c6
Source noteuspto-grants-2016_05