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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633888Generated: October 25, 2026

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

https://huagongshe.com/reaction/633888

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 numberUS09321769B2
Source datasetuspto-grants-2016_04
ORD IDord-19f0f10ba49c421285ef213c7e41f4c6
Source noteuspto-grants-2016_04