Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233701Generated: October 29, 2026

Cyclobutanone → Tert-butyl 4-(4-(1-cyanocyclobutylamino)phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2233701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantSodium SulfateHCID 24436—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactanttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 11011301—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-(1-cyanocyclobutylamino)phenyl)piperazine-1-carboxylateHCID 6713205484%

Reaction Steps

Trimethylsilyl cyanide (0.3 g, 3 mmol) was added dropwise to a mixture of 43a (0.415 g, 1.5 mmol), cyclobutanone (0.21 g, 3 mmol) and sodium sulfate (1 g) in dichloromethane (5 ml). The mixture was stirred for 15 hours. After filtration to eliminate sodium sulfate, the medium was concentrated under vacuum to obtain a brown liquid which was subjected to chromatography (dichloromethane:acetone, 75:25) to yield 43b (0.448 g, 1.26 mmol, 84%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709517B2
Source datasetuspto-grants-2010_05
ORD IDord-9a187d1afed64627b25c50988e892a7e
Source noteuspto-grants-2010_05