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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771143Generated: November 4, 2026

tert-Butyl piperazine-1-carboxylate → HCID 89838174, compound

https://huagongshe.com/reaction/1771143

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 4771099HCID 4771099—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventSodium BicarbonateHCID 516892—
ProductHCID 89838174HCID 89838174—

Reaction Conditions

Temperature20 °C

Reaction Steps

The synthesis is carried out in argon condition. 2.2 g (11.8 mmol) of N-Boc-piperazine and 2.5 g (11.8 mmol) of 3,5-dimethoxy-4-ethoxybenzaldehyde are mixed in 50 ml of dry of dichloromethane. After dissolution 2 drops of acetic acid is added, then 4.25 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, concentrated in vacuum at 50÷80° C. The residue (4.1 g of oil) is used on the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249115B2
Source datasetuspto-grants-2016_02
ORD IDord-6b917e080bec4743a2d3eccbad82cd91
Source noteuspto-grants-2016_02