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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121004Generated: October 29, 2026

1-Benzylpiperidin-4-ol → 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate

https://huagongshe.com/reaction/2121004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzylpiperidin-4-olHCID 78461—
Reactant1-Isocyanato-2-phenylbenzeneHCID 222280—
SolventAcetonitrileHCID 6342—
Product1-benzyl-4-piperidyl N-(2-biphenylyl)carbamateHCID 10500369—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a 50 ml sealed tube was added 2-biphenylylisocyanate (8 g, 41 mmol) in anhydrous acetonitrile (40 mL). To this solution was added N-benzyl-4-piperidinol (9.8 g, 51.25 mmol) and the tube was partially immersed in a silicon oil bath and heated to 85° C. After 16 h, the reaction mixture was cooled and concentrated in vacuo to give a 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693202B1
Source datasetuspto-grants-2004_02
ORD IDord-3ec7be5dc98543e8aec336d341004ed3
Source noteuspto-grants-2004_02