Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172230Generated: October 30, 2026

Ethanol → HCID 70873632, compound

https://huagongshe.com/reaction/2172230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-(4-Hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 11687740—
ReactantHCID 13683259HCID 13683259—
SolventWaterHCID 962—
ProductHCID 70873632HCID 7087363297%

Reaction Conditions

Temperature85 °C

Reaction Steps

2-[2-(Benzyloxy)ethyl]-2-methyloxirane (2.60 g, 13.5 mmol), 4-(4-hydroxyphenyl)piperazine-1-carboxylic acid tert-butyl ester (4.14 g, 14.9 mmol), tripotassium phosphate (1.15 g, 5.4 mmol) and ethanol (26 ml) were mixed and stirred at 80 to 90° C. overnight. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0→30:70) to afford the title compound as a pale yellow oil (6.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-0a8720b2b6a045378f4e8c9346b44758
Source noteuspto-grants-2015_06