HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1361187Erstellt: 24. Oktober 2026
Sodium methanesulfonate → 1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-one
https://huagongshe.com/de/reaction/1361187
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium methanesulfonate | HCID 638112 | — |
| Edukt | 1-(2-Bromothiazol-5-yl)propan-1-one | HCID 59278085 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-one | HCID 59278397 | — |
Reaktionsschritte
To a solution of 1-(2-bromo-thiazol-5-yl)-propan-1-one (75 mg, 0.34 mmol) in dimethyl sulfoxide (3 mL) was added the sodium methanesulfonate (41 mg, 0.34 mmol) followed by copper (I) iodide (65 mg, 0.34 mmol). The mixture was heated in a microwave at 120° C. for 1 hour. The reaction was diluted with EtOAc (20 mL) and washed with saturated aqueous sodium bicarbonate solution (50 mL) and brine (10 mL). The aqueous phase was extracted with EtOAc (2×10 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated to afford 1-(2-methanesulfonyl-thiazol-5-yl)-propan-1-one which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07879873B2 |
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| Quelldatensatz | uspto-grants-2011_02 |
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| ORD ID | ord-8357b378d7ea48b29f826b117a82ae3c |
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| Quellennotiz | uspto-grants-2011_02 |
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