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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968245Generated: October 29, 2026

1-Acetylpiperazine → Tert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamate

https://huagongshe.com/reaction/968245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22288418HCID 22288418—
SolventAcetic AcidHCID 176—
Solvent1,1-DichloroethaneHCID 6365—
SolventSodium BicarbonateHCID 516892—
ProductTert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamateHCID 22288425—

Reaction Steps

To a solution of tert-butyl 3-formyl-5-methylphenylcarbamate (200 mg, 0.85 mmol) and acetylpiperazine (131 mg, 1.02 mmol) in 0.1 mL HOAc and 4 mL dichloroethane was added NaBH(OAc)3 (216 mg, 1.02 mmol) at room temperature. After 2 hours additional acetylpiperazine (131 mg, 1.02 mmol) and NaBH(OAc)3 (216 mg, 1.02 mmol) were added. After 2 hours the mixture was diluted with saturated NaHCO3. The layers were separated and the aqueous extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (5% MeOH/CH2Cl2) gave tert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamate as a white foam:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958340B2
Source datasetuspto-grants-2005_10
ORD IDord-7ea9157a90f745ec8824265b942c1b79
Source noteuspto-grants-2005_10