Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023325Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → HCID 67327082, compound

https://huagongshe.com/reaction/1023325

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]BenzaldehydeHCID 53426168—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67327082HCID 6732708283.4%

Reaction Steps

To a 1,2-dichloroethane (15 mL) solution of 4-(2-{[tert-butyl(dimethyl)silyl]-oxy}ethyl)benzaldehyde (0.70 g) and tert-butyl piperazine-1-carboxylate (0.52 g) was added NaBH(OAc)3 (0.83 g) at 0° C. The resultant mixture was stirred at room temperature for 66 hours. To the reaction mixture was added saturated aqueous NaHCO3, and extracted with CH2Cl2. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=9/1 to 2/1) to afford tert-butyl 4-[4-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)benzyl]piperazine-1-carboxylate (0.96 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-c6bd434682d8483981fa1e73e1baa3a0
Source noteuspto-grants-2014_05