Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172253Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 70874679, compound

https://huagongshe.com/reaction/2172253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(4-Hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 11687740—
ReactantHCID 86709395HCID 86709395—
SolventEthanolHCID 702—
ProductHCID 70874679HCID 7087467956.2%

Reaction Steps

An ethanol solution (25.00 ml) of 20% sodium ethoxide was added to an ethanol solution (250 ml) of toluene-4-sulfonic acid (S)-4-(2-chloro-4-nitro-imidazol-1-yl)-2-hydroxybutyl ester (25.00 g), and the mixture was stirred at room temperature for 30 minutes. 4-(4-Hydroxyphenyl)piperazine-1-carboxylic acid tert-butyl ester (19.63 g) and tripotassium phosphate (13.61 g) were added to the reaction mixture, followed by heating under reflux for 4 hours. The reaction mixture was then concentrated under reduced pressure, and water was added to the residue, followed by extraction with methylene chloride. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate. After filtering, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride:ethyl acetate=1:0→methylene chloride:ethyl acetate=0:1) and concentrated under reduced pressure. Sodium hydride (3.08 g) was added to a dimethylformamide solution (269 ml) of residue and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture, followed by extraction with methylene chloride. The organic layer was dried over magnesium sulfate. After filtering, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride:ethyl acetate=1:0→methylene chloride:ethyl acetate=0:1) to afford the title compound as a yellow powder (16.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-a7353e6959c6496480e76c0056f4b3df
Source noteuspto-grants-2015_06