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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911393Generated: November 3, 2026

Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1911393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-cyclopropylpiperazine-1-carboxylateHCID 2029452468.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl piperazine-1-carboxylate (9.31 g, 50 mmol), [(1-ethoxycyclopropyl)oxy]trimethylsilane (20.11 mL, 100.00 mmol) and acetic acid (14.31 mL, 250.00 mmol) in tetrahydrofuran (100 mL), methanol (10 mL) was treated with sodium cyanoborohydride (4.71 g, 75.00 mmol) at 20° C. The resulting solution was stirred at 60° C. for 18 h. The reaction mixture was cooled, filtered and evaporated to dryness. 1N HCl (40 ml) and water (60 ml) were added and the solution extracted with ethyl acetate (3×50 ml). The aqueous layer was basified to pH 10 with solid potassium carbonate and extracted with ethyl acetate (4×50 ml). The organic extracts were washed with saturated sodium chloride solution (50 ml) and dried over MgSO4, filtered and evaporated to dryness to give tert-butyl 4-cyclopropylpiperazine-1-carboxylate (7.73 g, 68.3%) as a white waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-d7e9e4ca936c4c6bb6ac10f7d8f91bb9
Source noteuspto-grants-2013_12