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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831801Generated: October 27, 2026

Ethyl Acetate → tert-butyl N-[(1-cyanopiperidin-4-yl)methyl]carbamate

https://huagongshe.com/reaction/1831801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
SolventAcetonitrileHCID 6342—
Producttert-butyl N-[(1-cyanopiperidin-4-yl)methyl]carbamateHCID 23396324—

Reaction Steps

Piperidin-4-ylmethyl-carbamic acid tert-butyl ester (4 g, 18.66 mmol) was suspended in 120 ml of acetonitrile. Dried potassium carbonate (2.837 g, 20.53 mmol) was added. A solution of bromoacetonitrile in (3.72 ml, 5 mmolar solution, 18.66 mmol) was added (argon atmosphere) and the mixture was stirred for 3 hours. After addition of aqueous FeSO4 solution and ethyl acetate, the separated solid was filtered and the organic layer separated, dried and evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067665B2
Source datasetuspto-grants-2006_06
ORD IDord-724c546b1ff04290aeae174fc648cf90
Source noteuspto-grants-2006_06