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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157319Generated: November 4, 2026

Chloroacetonitrile → Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1157319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductTert-butyl 4-(cyanomethyl)piperazine-1-carboxylateHCID 21936030—

Reaction Steps

To a stirred solution of N-Boc piperazine (1 g) in dry THF (20 ml), triethylamine (3 ml), followed by chloroacetonitrile (5.02 ml) were added dropwise. The reaction mixture was allowed to stir at room temperature for overnight. The solvent was removed under vacuum and residue was diluted ethyl acetate (20 ml). The organic layer was concentrated to dryness under reduced pressure to afford tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate, which was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-7f645550e2b74a4886aa6b6fc1f29716
Source noteuspto-grants-2010_10