HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182252Generated: October 26, 2026
Ethyl Acetate → Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2182252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Fluorobenzonitrile | HCID 14517 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate | HCID 2795512 | 23.4% |
Reaction Steps
A mixture of 4-fluorobenzonitrile (3.6 g) and N-tert-butyloxycarbonylpiperazine (5.58 g) in acetonitrile (60 mL) was heated at 80° C. for 72 hours. The reaction mixture was then cooled to room temperature and then treated with a mixture of sodium bicarbonate solution and ethyl acetate (300 mL, 1:1, v/v). The organic phase was separated and then evaporated. The residue was subjected to chromatography on silica gel eluting with a mixtures of heptane and ethyl acetate (from 3:7 to 1:1, v/v) to give the title compound (2 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897207B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-f4f68f795977483f93ab1318de38b4c5 |
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| Source note | uspto-grants-2005_05 |
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