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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171988Generated: November 3, 2026

Triethylamine → tert-butyl 2-[(Z)-N'-hydroxycarbamimidoyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/2171988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantTert-butyl 2-cyanopiperidine-1-carboxylateHCID 2756784—
SolventEthanolHCID 702—
Producttert-butyl 2-[(Z)-N'-hydroxycarbamimidoyl]piperidine-1-carboxylateHCID 4583340095%

Reaction Steps

In a 16 mL vial, N-boc-2-cyanopiperidine (500 mg, 2.38 mmol) was dissolved in ethanol (6.7 mL), then hydroxylamine hydrochloride (231 mg, 3.33 mmol) and triethylamine (0.56 mL, 4.05 mmol) were added. The reaction mixture was stirred at reflux for 5 h, cooled and concentrated. The residue was taken up in EtOAc and water. The two layers were separated and the aqueous phase extracted with EtOAc. The combined organics were dried on Na2SO4 and concentrated to give the product as a white solid (550 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051321B2
Source datasetuspto-grants-2015_06
ORD IDord-71232b33b45241d9aa87c6ec2bec74d4
Source noteuspto-grants-2015_06