HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5325Erstellt: 23. Oktober 2026
1,1-Dibromoethane → 2-Imino-3-(3-trifluoromethylphenyl)thiazolidine
https://huagongshe.com/de/reaction/5325
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,1-Dibromoethane | HCID 11201 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(Trifluoromethyl)phenylthiourea | HCID 735844 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-Imino-3-(3-trifluoromethylphenyl)thiazolidine | HCID 22416978 | 110% |
Reaktionsschritte
A solution of N-(3-trifluoromethylphenyl)thiourea (6.1 g), dibromoethane (5.7 g) and anhydrous potassium carbonate (11.5 g) in acetone (60 ml) was refluxed for 1 day. The solvent was removed by distillation therefrom, and the residue was extracted with ethyl ether, washed with water, dried over anhydrous magnesium sulfate and subjected to column chromatography to give 7.5 g of 2-imino-3-(3-trifluoromethylphenyl)thiazolidine. The thus obtained 2-imino-3-(3-trifluoromethylphenyl)thiazolidine (1.0 g), n-butyl chlorocarbonate (0.61 g) and triethylamine (1.2 g) were dissolved in tetrahydrofuran, and the resultant solution was stirred at room temperature for 5 hours. The solvent was removed, and the residue was extracted with ethyl acetate, washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.57 g of 2-butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05244863 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-7abe0b247b3646b18c986acb76de854f |
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| Quellennotiz | uspto-grants-1993_09 |
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