Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694918Generated: November 2, 2026

Water → 4-[2-(3-Methoxypropoxy)phenyl]-2,2-dimethylpiperazine-1-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/1694918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-[2-(3-Methoxypropoxy)phenyl]-2,2-dimethyl-5-oxopiperazine-1-carboxylic acid t-butyl esterHCID 66645509—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(3-Methoxypropoxy)phenyl]-2,2-dimethylpiperazine-1-carboxylic acid t-butyl esterHCID 6664562794.7%

Reaction Steps

2.30 ml of a borane-tetrahydrofuran complex (1.2 mol/l) (2.76 mmol) was added to a solution of 303 mg of 4-[2-(3-methoxypropoxy)phenyl]-2,2-dimethyl-5-oxopiperazine-1-carboxylic acid t-butyl ester obtained in Example (10e) (0.77 mmol) in tetrahydrofuran (2.8 ml) under a nitrogen atmosphere and under ice-cooling over five minutes, and the mixture was stirred at room temperature for 15 minutes. The reaction mixture was cooled in an ice bath. Then, 2.76 ml of a 1 N sodium hydroxide aqueous solution (2.76 mmol) was slowly added and the mixture was further stirred at room temperature for one hour. Water was added to the reaction mixture, followed by extraction with ethyl acetate. Then, the organic layer was washed with water and brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent:n-hexane/ethyl acetate=30/1-10/1) to obtain 276 mg of the title compound (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-22f1a752d48b4a07ad46c953ddfcb5f4
Source noteuspto-grants-2012_04