Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771139Generated: October 30, 2026

tert-Butyl piperazine-1-carboxylate → HCID 89838520, compound

https://huagongshe.com/reaction/1771139

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantBenzaldehyde, 2,3,4-triethoxy-HCID 19956854—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 89838520HCID 89838520—

Reaction Conditions

Temperature20 °C

Reaction Steps

The synthesis is carried out in argon condition. 1.1 g (5.9 mmol) of N-Boc-piperazine and 1.40 g (5.9 mmol) of 2,3,4-triethoxybenzaldehyde are mixed in 25 ml of dry dichloromethane. After dissolution 2 drops of acetic acid is added, then 2.12 g (10 mmol) of NaBH(OAc)3 is added and the mixture is stirred for 12 h at 20° C. Then 10 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 (2.2 g of yellowish oil) is used on the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249115B2
Source datasetuspto-grants-2016_02
ORD IDord-d62b6eb34aa44fea8b6513ab94e67292
Source noteuspto-grants-2016_02