HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245001Generated: October 26, 2026
Ethylene Glycol → tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/245001
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate | HCID 11011301 | 43.3% |
Reaction Steps
A mixture of 4-iodoaniline (0.654 g, 3 mmol), piperazine-1-carboxylic acid tert-butyl ester (0.67 g, 3.6 mmol), potassium phosphate (1.272 g, 6 mmol), ethylene glycol (0.33 ml) and copper iodide (0.03 g, 0.15 mmol) in 2-propanol (3 ml) was placed under argon in a sealed-tube and heated to 80° C. for 30 hours. After being cooled to room temperature, the medium was washed with water (50 ml) and extracted with ethyl acetate (100 ml). The organic layer was dried over MgSO4, concentrated and chromatographed (dichloromethane:acetone, 70:30) to yield 43a (0.36 g, 1.3 mmol, 43%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658681B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-21cc155a42d14e5c9f54ed5339bb73ba |
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| Source note | uspto-grants-2014_02 |
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