HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533859Generated: October 26, 2026
Potassium Hydroxide → 1-(2-Fluoro-6-methoxyphenyl)piperazine
https://huagongshe.com/reaction/1533859
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Fluoro-6-methoxyaniline | HCID 459253 | — |
| Reactant | Ethanamine, 2-bromo-N-(2-bromoethyl)-, hydrobromide (1:1) | HCID 12692731 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Fluoro-6-methoxyphenyl)piperazine | HCID 15676121 | 77% |
Reaction Steps
2-Fluoro-6-methoxyaniline (7.80 g) and 17.23 g of di-(2-bromoethyl)amine hydrobromide were dissolved in 5 ml of water and, by heating at about 110° C. on a bath, 10 ml of 30% potassium hydroxide solution was added thereto (each about 3.5 ml once an hour). Heating was further continued (7 hours in total). After cooled, the reaction solution was made alkaline with aqueous solution of sodium hydroxide to salt out and extracted with chloroform twice. The extract was washed with saturated sodium chloride solution, dried over sodium sulfate, the solvent was evaporated therefrom, and the residue was purified by a column chromatography to give 8.95 g of oily 1-(2-fluoro-6-methoxyphenyl)piperazine in 34.93 g yield or 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05086049 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-4221356c531047a2a9f8568c1e0db29d |
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| Source note | uspto-grants-1992_02 |
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