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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872356Generated: November 3, 2026

Water → 1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazine

https://huagongshe.com/reaction/1872356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 11687740—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazineHCID 21182449—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of 1-(4-Hydroxyphenyl)-4-tert-butoxycarbonylpiperazine (3 g) and potassium carbonate (0.82 g) in N,N-dimethylformamide (15 ml) was added octyl bromide (1.87 ml). The mixture was stirred for 10 hours at 70° C. The reaction mixture was added to a mixture of water and ethyl acetate. The organic layer was taken, and dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel, and eluted with (hexane : ethyl acetate=9:1). The fractions containing the object compound were combined, and evaporated under reduced pressure to give 1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazine (2.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107458
Source datasetuspto-grants-2000_08
ORD IDord-ea45349c290b44c88997654852ac3161
Source noteuspto-grants-2000_08