HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 236283Erstellt: 24. Oktober 2026
Diethyl Ether → 2-Sulfanylidene-1,3-thiazolidine-3-carbonyl chloride
https://huagongshe.com/de/reaction/236283
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Phosgene | HCID 6371 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | HCID 178527880 | HCID 178527880 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Sulfanylidene-1,3-thiazolidine-3-carbonyl chloride | HCID 23506666 | 65.531,898% |
Reaktionsschritte
A solution of 2-mercaptothiazoline (2.0 g, 0.0168 mmol) and Et3N (2.9 ml, 0.021 mol) in THF (30 ml) was added dropwise to a solution of phosgene (2.37 g, 0.0239 mol) in toluene (12 ml) at 5° C. for 7 min. The mixture was stirred at 5° C. for 5 min and then filtered to remove the precipitate. The filtrate was evaporated in vacuo to give a crystalline residue. To the residue was added ether (10 ml) and the ether was evaporated in vacuo. This operation was repeated twice. 2-Thioxo-3-thiazolidinecarbonyl chloride (2,0 g) was obtained as a solid. 65.5% yield. IR (Nujol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04643991 |
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| Quelldatensatz | uspto-grants-1987_02 |
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| ORD ID | ord-38183b71ef304e3ba36e202eb35f3851 |
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| Quellennotiz | uspto-grants-1987_02 |
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