Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644734Generated: October 30, 2026

Sodium Bicarbonate → tert-butyl (2S)-2-methyl-4-[2-methyl-4-(methylamino)benzyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/644734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
Reactant2-Methyl-4-(methylamino)benzaldehydeHCID 45083649—
Solvent1,2-DichloroethaneHCID 11—
Producttert-butyl (2S)-2-methyl-4-[2-methyl-4-(methylamino)benzyl]piperazine-1-carboxylateHCID 5926212937%

Reaction Steps

To a mixture of 2-methyl-4-(methylamino)benzaldehyde (D93) (0.397 g) and 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate (0.533 g, 2.66 mmol) in 1,2-DCE (35 mL) was added sodium tri(acetoxy)borohydride (0.847 g, 4.00 mmol) and the reaction stirred at room temperature overnight. Saturated aqueous NaHCO3 (30 mL) was added and the mixture was stirred for 4 h. The reaction mixture was extracted with DCM and the organics were dried and concentrated to give the crude product which was purified by column chromatography. Elution with ether/petroleum ether gave the title compound as a colourless oil (0.328 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700599B2
Source datasetuspto-grants-2010_04
ORD IDord-65322071637a4902afa7c0362b7d491e
Source noteuspto-grants-2010_04