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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | p-(1-Piperazinyl)phenol | HCID 92467 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 4-(2-hydroxyphenyl)piperazine-1-carboxylate | HCID 19034142 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648368 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-87ec6e79614e406cac5ae73afa6d6f1a |
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| Source note | uspto-grants-1997_07 |
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