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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362115Generated: November 1, 2026

Acetic Acid → HCID 66967695, compound

https://huagongshe.com/reaction/1362115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl oxoacetateHCID 70211—
Reactant1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductHCID 66967695HCID 6696769538%

Reaction Steps

A solution of 4-(3-aminopropyl)-1-methylpiperazine (3.1 mL, 20 mmol) in MeOH (50 mL) was cooled in an ice bath and treated with ethyl glyoxylate (50% solution in toluene, 5.6 mL, 27 mmol) and AcOH (3 mL). After stirring for 15 min, NaBH3CN (1.37 g, 21.8 mmol) was added and the mixture was allowed to stir for 7 h while slowly warming to room temperature. The mixture was diluted with saturated aqueous NaHCO3 (150 mL) and then extracted with EtOAc (3×100 mL) followed by CH2Cl2 (3×100 mL). The combined CH2Cl2 layers were dried over Na2SO4, filtered and the solvent was removed in vacuo to give the title compound (1.81 g, 38%) as a colorless oil: MS (ESI) m/e 244 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-ff134c5721a34500b75ba7e14f626b95
Source noteuspto-grants-2011_02