HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389278Generated: October 26, 2026
1-Piperazinecarboxylic acid, ethyl ester → Ethyl 4-[2-(4-fluorophenyl)ethyl]piperazine-1-carboxylate
https://huagongshe.com/reaction/1389278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Piperazinecarboxylic acid, ethyl ester | HCID 8431 | — |
| Reactant | 4-Fluorophenethyl bromide | HCID 573153 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-[2-(4-fluorophenyl)ethyl]piperazine-1-carboxylate | HCID 12679858 | 91% |
Reaction Steps
A mixture of 80 g 1-(ethoxycarbonyl)piperazine and 41 g of 2-(4-fluorophenyl)ethyl bromide is kept at room temperature overnight and then heated to 100° C. for 1 hour. After cooling, it is diluted with 50 ml water and extracted with benzene. The extract is washed with water and then shaken with 5% hydrochloric acid. The separated solid hydrochloride is filtered off, washed with a small quantity of water, decomposed by treatment with aqueous ammonia and the base isolated again by extraction with benzene. Processing of the extract affords 51 g (91%) of the crude 1-(ethoxycarbonyl)-4-(2-[4-fluorophenyl]ethyl)piperazine, b.p. 198° C./3 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243805 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-c7a1a6380ce448c7853ba59a71e45744 |
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| Source note | uspto-grants-1981_01 |
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