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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771140Generated: November 4, 2026

tert-Butyl piperazine-1-carboxylate → HCID 89838245, compound

https://huagongshe.com/reaction/1771140

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Tert-butyl-4-methoxybenzaldehydeHCID 3774604—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 89838245HCID 89838245—

Reaction Conditions

Temperature20 °C

Reaction Steps

The synthesis is carried out in argon condition. 2 g (10.7 mmol) of N-Boc-piperazine and 2.06 g (10.7 mmol) of 3-tert-butyl-4-methoxybenzaldehyde are mixed in 30 ml of dry dichloromethane. After dissolution 2 drops of acetic acid is added, then 4.24 g (20 mmol) of NaBH(OAc)3 is added and the mixture is stirred for 12 h at 20° C. Then 20 ml of 5% NaHCO3 aqueous solution is added dropwise with care to the reaction mixture. The organic layer is separated, washed with 5% Na2CO3 solution, dried over sodium sulfate, filtered off and concentrated in vacuum at 50÷80° C. The residue (3.5 g of yellow oil) is used on the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249115B2
Source datasetuspto-grants-2016_02
ORD IDord-ca309766a7ba40cb872c77b83d3d0e2f
Source noteuspto-grants-2016_02