HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437232Generated: October 31, 2026
Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate
https://huagongshe.com/reaction/1437232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | (1-Ethoxycyclopropoxy)trimethylsilane | HCID 2734686 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl 4-cyclopropylpiperazine-1-carboxylate | HCID 20294524 | 71% |
Reaction Steps
Piperazine-1-carboxylic acid tert-butyl ester (1.87 g), [(1-ethoxycyclopropyl)oxy]trimethylsilane (8.05 mL), and acetic acid (5.72 mL) were dissolved in methanol (60 mL). To the resultant solution, sodium cyanoborohydride (1.89 g) was added at room temperature, followed by stirring for 5 days. Diethyl ether was added to the residue obtained by removal through evaporation of the reaction solvent under reduced pressure, and insoluble matter was filtered off. The filtrate was partitioned by addition of aqueous 1N sodium hydroxide thereto. The organic layer was washed with saturated brine, and then dried over magnesium sulfate anhydrate, followed by filtration. The solvent was evaporated under reduced pressure. The residue was purified through silica gel column chromatography (hexane-ethyl acetate), to thereby give the title compound as a solid (1.62 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07622471B2 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-ba5d1e9c2020473cb238c63d6d851666 |
|---|
| Source note | uspto-grants-2009_11 |
|---|