HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16783Generated: October 25, 2026
Acetic Acid → Tert-butyl 4-cyclobutylpiperazine-1-carboxylate
https://huagongshe.com/reaction/16783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-cyclobutylpiperazine-1-carboxylate | HCID 57423951 | 53.5% |
Reaction Steps
Water (0.3 mL), cyclobutanone (2.000 g, 28.53 mmol) and acetic acid (3.48 mL, 60.86 mmol) were added to a stirred solution of tert-butyl piperazine-1-carboxylate (3.54 g, 19.02 mmol) in THF (40 mL) under nitrogen. Sodium cyanoborohydride (1.793 g, 28.53 mmol) was added portionwise over a period of 10 mins. The resulting mixture was stirred at 60° C. for 19 h. The reaction mixture was evaporated to dryness and mixed with water (80 mL) and 1M HCl (25 mL). The solution was washed with EtOAc (2×50 mL), basified with K2CO3 and extracted with EtOAc (2×30 mL). The organic layer was washed with saturated brine and dried over MgSO4, filtered and evaporated to afford pure tert-butyl 4-cyclobutylpiperazine-1-carboxylate (2.445 g, 53.5%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07737149B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-d9ddea175d7547909e7151d1e5cfebeb |
|---|
| Source note | uspto-grants-2010_06 |
|---|