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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

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 20294524127%

Reaction Conditions

Temperature63 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208497B2
Source datasetuspto-grants-2007_04
ORD IDord-58f0c5cc083d43e4ab86a819a00e10a9
Source noteuspto-grants-2007_04