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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714116Generated: November 3, 2026

Sodium Hydroxide → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1714116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-cyclopropylpiperazine-1-carboxylateHCID 20294524—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of tert-butyl piperazine-1-carboxylate (75.0 g), THF (500 mL), methanol (500 mL), [(1-ethoxycyclopropyl)oxy]trimethylsilane (161 mL), NaBH3CN (38.0 g), and acetic acid (37 mL) was heated at 60° C. for 5 h. The mixture was cooled to room temperature, treated with water (30 mL) and stirred for 5 min. The mixture was then treated with 1 N NaOH (130 mL) and was further stirred for 15 min. The mixture was concentrated, and the remaining aqueous solution was extracted with CH2Cl2 (500 mL). The organic layer was washed with 1 N NaOH (500 mL). The combined aqueous layers were extracted with CH2Cl2 (150 mL). The combined organic layers were washed with brine (400 mL), dried (Na2SO4), and concentrated to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795426B2
Source datasetuspto-grants-2010_09
ORD IDord-a7bf55e20f61452f8439bb869ec5ec51
Source noteuspto-grants-2010_09