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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265902Generated: October 30, 2026

Tetrahydrofuran → Benzyl 4-(2-hydroxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/265902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactantp-(1-Piperazinyl)phenolHCID 92467—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-(2-hydroxyphenyl)piperazine-1-carboxylateHCID 19034142—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Piperazinyl phenol (Schweizerhall, 5 g, 30.5 mmol) was dissolved in THF (150 mL), treated with diisopropylethylamine (12.2 mL, 70.0 mmol), and cooled to 0° C. Benzylchloroformate (4.4 mL, 30.5 mmol) was added and the reaction was allowed to warm to room temperature and stir overnight. The solution was diluted with EtOAc, washed with water and brine, dried over MgSO4, filtered and evaporated to give a brown oil. Column chromatography (SiO2, 40% EtOAc/hexanes) gave 28-2 as a white solid. Rf (40% EtoAc/hexanes) 0.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648368
Source datasetuspto-grants-1997_07
ORD IDord-87ec6e79614e406cac5ae73afa6d6f1a
Source noteuspto-grants-1997_07