HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272033Generated: October 31, 2026
Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate
https://huagongshe.com/reaction/1272033
Participants
| Role | Name | HCID | Charge |
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| 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 | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-cyclopropylpiperazine-1-carboxylate | HCID 20294524 | 127% |
Reaction Steps
To a solution of 1-tert-butyloxycarbonylpiperazine (1.16 g, 6.23 mmol) in THF (10 ml) and methanol (5 ml) were added 1-ethoxy-1-trimethylsilyloxycyclopropane (2.40 ml, 12.0 mmol), acetic acid (0.75 ml), and sodium cyanoborohydride (7.8 ml of a 1M solution in THF, 7.8 mmol), and the mixture was stirred at 63° C. for 16 hours. The mixture was concentrated under reduced pressure, and the residue was mixed with water (20 ml) and potassium carbonate (6.6 g). The product was extracted with ethyl acetate (3×30 ml), the combined extracts were dried over magnesium sulphate, and concentrated under reduced pressure. 1.79 g (100%) of the title compound was obtained as an oil, which completely crystallized after a few hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208497B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-58f0c5cc083d43e4ab86a819a00e10a9 |
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| Source note | uspto-grants-2007_04 |
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