HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655598Erstellt: 24. Oktober 2026
Sodium Iodide → 4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester
https://huagongshe.com/de/reaction/655598
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 4-(2-Chloroethyl)-1,2-dimethoxybenzene | HCID 3015359 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester | HCID 66995785 | 76,5% |
Reaktionsschritte
A reaction mixture of 4-(2-chloroethyl)-1,2-dimethoxybenzene (3.6 g, 17.9 mmol), piperazine-1-carboxylic acid t-butyl ester (4.0 g, 21.5 mmol), K2CO3 (4.97 g, 36 mmol), and NaI (2.7 g, 18 mmol) in DMF (20 mL) was stirred at 80° C. for 3 h, cooled to room temperature, and partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by column chromatography to afford 4-[2-(3,4-dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester (4.8 g, 76%) which was dissolved in 4 N HCl in dioxane. This solution was stirred at room temperature for 4 h, concentrated, and dried in a high vacuum oven to give the title compound quantitatively.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08071602B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-5f9829d032d24b5a9f7bd5cfe5515bc6 |
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| Quellennotiz | uspto-grants-2011_12 |
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