HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32199Erstellt: 23. Oktober 2026
Allyl bromide → 1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
https://huagongshe.com/de/reaction/32199
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazine | HCID 11992284 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane ethylacetate | HCID 21226138 | — |
| Produkt | 1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine | HCID 23141803 | — |
Reaktionsschritte
A mixture of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (30 mg, 0.1 mmol) produced in Example (8b), allyl bromide (14.8 mg, 0.12 mmol), potassium carbonate (20.8 mg, 0.15 mmol) and dimethylformamide (1 mL) was stirred for 4 hours and 20 minutes at an external temperature of 80° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with ethyl acetate-dichloromethane. The separated organic layer was washed with water, and then the solvent was distilled off by nitrogen stream. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425554B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-00d379097aaf48f39b85028bf376efd8 |
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| Quellennotiz | uspto-grants-2008_09 |
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