HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380516Generated: October 25, 2026
1-Piperazinecarboxaldehyde → 1-(2-(4-Bromophenoxy)ethyl)piperazine
https://huagongshe.com/reaction/1380516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | 2-Bromoethyl p-bromophenyl ether | HCID 87797 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(2-(4-Bromophenoxy)ethyl)piperazine | HCID 23325337 | 70.1% |
Reaction Steps
A mixture of 56.0 g (0.2 moles) of 2-bromoethyl p-bromophenyl ether and 45.6 g (0.4 moles) of 1-formylpiperazine in 500 ml of 2-propanol was heated at reflux for 18 hours. The mixture was cooled and filtered. The filter was washed with 2-propanol and the filtrate was evaporated to an oil in vacuo. Water was added and the oil was extracted three times with about 200 ml of chloroform. The extracts were combined, dried over magnesium sulfate and filtered. The filtrate was evaporated to an oil to which 250 ml of 5N sodium hydroxide was added. The mixture was refluxed for 18 hours, cooled and extracted three times with about 200 ml of chloroform. The extracts were combined, dried over magnesium sulfate and evaporated to an oil. The oil was distilled, bp 125°-128° C./0.05 mm of mercury, and gave 40 g of 1-[2-(4-bromophenoxy)ethyl]-piperazine as a yellowing oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04582833 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-89c66b7559a24da19ea8459291569b95 |
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| Source note | uspto-grants-1986_04 |
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