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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16824Generated: October 25, 2026

Acetic Acid → Tert-butyl 4-cyclobutylpiperazine-1-carboxylate

https://huagongshe.com/reaction/16824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclobutanoneHCID 14496—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-cyclobutylpiperazine-1-carboxylateHCID 5742395150.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

Water (0.15 mL), cyclobutanone (1 g, 14.27 mmol) and acetic acid (1.742 mL, 30.44 mmol) were added to a stirred solution of tert-butyl piperazine-1-carboxylate (1.772 g, 9.51 mmol) in THF (20 mL) under nitrogen. Sodium cyanoborohydride (0.897 g, 14.27 mmol) was added portion wise over a period of 10 mins. The resulting mixture was stirred at 60° C. for 20 h. The reaction mixture was evaporated to dryness and mixed with water (40 mL) and 1M HCl (15 mL). The solution was washed with EtOAc (2×25 mL), basified with solid K2CO3 and extracted with EtOAc (2×15 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 (1.155 g, 50.5%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-434fd138f4dd4c9a82375bc7ddcf52ad
Source noteuspto-grants-2010_06