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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1,4-Bis(t-butoxycarbonyl)-2-(2-bromoethyl)piperazine | HCID 22710728 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,4-Bis(tert-butoxycarbonyl)-2-(2-cyanoethyl)piperazine | HCID 22710199 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747023B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-0a66c9f0c40746e19510fbcf077bc6db |
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| Source note | uspto-grants-2004_06 |
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