HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336832Erstellt: 24. Oktober 2026
Water → Tert-butyl 4-(4-formyl-2-methoxyphenyl)piperazine-1-carboxylate
https://huagongshe.com/de/reaction/336832
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 4-Fluoro-3-methoxybenzaldehyde | HCID 2737358 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | Tert-butyl 4-(4-formyl-2-methoxyphenyl)piperazine-1-carboxylate | HCID 86671380 | 51% |
Reaktionsschritte
To 400 mg (2.60 mmol) of 4-fluoro-3-methoxybenzaldehyde diluted in 10 ml of dimethylsulfoxide are respectively added 483 mg (2.60 mmol) of tert-butyl piperazine-1-carboxylate, then 394 mg (2.85 mmol) of potassium carbonate. The solution is heated to 90° C. for 40 h, then water is added and the product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate, and concentrated. The residue obtained is purified by chromatography on silica (cyclohexane/ethyl acetate eluent: 8:2) to yield 425 mg of tert-butyl 4-(4-formyl-2-methoxyphenyl)piperazine-1-carboxylate in the form of a colourless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889711B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-d758faf30d914d1d943e1c7686ed1efc |
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| Quellennotiz | uspto-grants-2014_11 |
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