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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906363Generated: October 28, 2026

Formaldehyde → 1,1-Dimethylethyl (2S)-2-methyl-4-{[4-(methylamino)phenyl]methyl}-1-piperazinecarboxylate

https://huagongshe.com/reaction/906363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactant1,1-Dimethylethyl (2S)-4-[(4-aminophenyl)methyl]-2-methyl-1-piperazinecarboxylateHCID 59262217—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
Product1,1-Dimethylethyl (2S)-2-methyl-4-{[4-(methylamino)phenyl]methyl}-1-piperazinecarboxylateHCID 59262131—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1,1-dimethylethyl (2S)-4-[(4-aminophenyl)methyl]-2-methyl-1-piperazinecarboxylate (D22) (7.45 g, 24.43 mmol), paraformaldehyde (2.202 g, 73.28 mmol) and sodium methoxide (6.597 g, 122.13 mmol) in MeOH (150 mL) under an argon atmosphere was heated at 50° C. over-weekend. After cooling, sodium borohydride (1.848 g, 48.85 mmol) was added and the reaction mixture was heated at 50° C. for 1 h then cooled to room temperature. Acetone was added until no more bubbling was observed, then the mixture was concentrated. The residue was partitioned between DCM and water and the aqueous was re-extracted with DCM. The combined organics were diluted with MeOH (approx 20 mL) to aid solubility, dried and concentrated to yield the title compound as an off white solid (7.77 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012981B2
Source datasetuspto-grants-2011_09
ORD IDord-1ba91d565950454f9540694219a12c38
Source noteuspto-grants-2011_09