HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129206Erstellt: 24. Oktober 2026
Hydrochloric Acid → 4,4-Difluoro-1-[5-chloro-2-thienyl]-butane-1,3-dione
https://huagongshe.com/de/reaction/129206
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl difluoroacetate | HCID 9961 | — |
| Edukt | 2-Acetyl-5-chlorothiophene | HCID 80572 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,4-Difluoro-1-[5-chloro-2-thienyl]-butane-1,3-dione | HCID 18920366 | 97,2% |
Reaktionsschritte
Ethyl difluoroacetate (3.51 g, 28.3 mmol) was placed in a 100 mL round bottom flask and dissolved in ether (10 mL). To the stirred solution was added 25 weight % sodium methoxide (6.12 g, 28.3 mmol) followed by 2-acetyl-5-chlorothiophene (4.12 g, 25.6 mmol). A pink precipitate formed after 5 minutes which was dissolved by adding ether (10 mL) and THF (10 mL) to the reaction. The reaction was stirred at room temperature overnight (15.75 hours), then treated with 3N HCl (15 mL). The organic layer was collected and washed with brine (20 mL), dried over MgSO4, and concentrated in vacuo to give a red solid (5.94 g) which was recrystallized from methylene chloride/isooctane to give the like diketone as a yellow solid (2.02 g, mp 72°-77° C., 33% ). 1H NMR (CDCl3) 300 MHz 14.60 (br s, 1H), 7.57 (d, J=4.2 Hz, 1H), 7.01 (d, J=4.2 Hz, 1H), 6.32 (s, 1H), 6.04 (t, J=54.2 Hz, 1H); 19F NMR (CDCl3) 300 MHz: -127.01 (d); M+238.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05466823 |
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| Quelldatensatz | uspto-grants-1995_11 |
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| ORD ID | ord-ef54652ad4394685a63565ac3755ddd9 |
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| Quellennotiz | uspto-grants-1995_11 |
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