HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56613Erstellt: 23. Oktober 2026
2-Bromo-4'-nitroacetophenone → 3-[2-(4-Nitrophenyl)-2-oxoethyl]-1,3-thiazolidine-2,4-dione
https://huagongshe.com/de/reaction/56613
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromo-4'-nitroacetophenone | HCID 66840 | — |
| Edukt | 1,3-Thiazolidine-2,4-dione potassium salt | HCID 87892318 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 3-[2-(4-Nitrophenyl)-2-oxoethyl]-1,3-thiazolidine-2,4-dione | HCID 11550894 | — |
Reaktionsschritte
A little at a time, 1.3 g (8.4 mmol) of 1,3-thiazolidine-2,4-dione potassium salt were added to a solution of 2.0 g (8.2 mmol) of 2-bromo-1-(4-nitrophenyl)ethanone in 80 ml of acetone, and the mixture was stirred at 60° C. for 1 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water/dichloromethane. After phase separation, the organic phase was dried (sodium sulphate), filtered, concentrated under reduced pressure and dried. Yield: 2.3 g (98% of theory)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434690B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-d1249409e06848c98d2c30682af412d3 |
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| Quellennotiz | uspto-grants-2016_09 |
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