HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16745Erstellt: 24. Oktober 2026
5-Bromothiophene-2-carbaldehyde → Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylate
https://huagongshe.com/de/reaction/16745
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Bromothiophene-2-carbaldehyde | HCID 78428 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylate | HCID 28065298 | 73% |
Reaktionsschritte
A mixture of 5-bromothiophene-2-carboxaldehyde (3.82 g, 20.0 mmol), tert-butyl piperazine-1-carboxylate (4.1 g, 22.0 mmol), N-ethyl-N,N-diisopropylamine (7.0 ml, 40.0 mmol) and dimethylsulphoxide (5.0 ml) were stirred at 130° C. under an atmosphere of nitrogen for 18 h. The cooled mixture was partitioned between ethyl acetate and water. The organics were washed with water, brine, dried over magnesium sulphate and evaporated. The resultant dark red solid was purified by silica column chromatography, eluting with dichloromethane followed by ethyl acetate/dichloromethane (15%) to give tert-butyl 4-(5-formylthien-2-yl)piperazine-1-carboxylate (4.3 g, 73%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737149B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-c417a6ea2d5f4f54842f9fa9a25eed89 |
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| Quellennotiz | uspto-grants-2010_06 |
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