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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352889Generated: November 1, 2026

Potassium Cyanide → 1,4-Bis(tert-butoxycarbonyl)-2-(2-cyanoethyl)piperazine

https://huagongshe.com/reaction/352889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant1,4-Bis(t-butoxycarbonyl)-2-(2-bromoethyl)piperazineHCID 22710728—
SolventEthanolHCID 702—
Product1,4-Bis(tert-butoxycarbonyl)-2-(2-cyanoethyl)piperazineHCID 22710199—

Reaction Conditions

Temperature110 °C

Reaction Steps

To an aqueous solution (3.0 ml) of potassium cyanide (85.0 mg) was added a solution of 1,4-bis(t-butoxycarbonyl)-2-(2-bromoethyl)piperazine (393 mg) in ethanol (3.0 ml), followed by stirring under heat at 110° C. for 3 hours. After the removal of ethanol by distillation under reduced pressure, methylene chloride (100 ml) was added to the residue. The organic layer was washed with distilled water until the water phase became neutral. The resulting organic layer was washed with saturated aqueous NaCl solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column (silica gel 15 g, hexane:ethyl acetate=2:1), whereby the title compound (145.0 mg, 43%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-0a66c9f0c40746e19510fbcf077bc6db
Source noteuspto-grants-2004_06