HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Fluorothiophenol → Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Fluorothiophenol | HCID 520216 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | HCID 19736751 | HCID 19736751 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate | HCID 19927552 | 82,2% |
Reaktionsschritte
The crude product from Step A (3.9 g, 20 mole) was taken up in 20 ml of ethanol. To this solution, being stirred at room temperature, was added 2-fluorothiophenol (2.5 g, 20 mmole) and 50 mg of solid sodium ethoxide. After stirring for eight hours the ethanol was concentrated and the residue taken up in ether. The ether mixture was washed twice with 15% NaOH solution, dried (MgSO4) and concentrated to a colorless oil (5.3 g, 82% yield). 1H NMR (CDCl3) δ: 7.28 (4H, m), 7.06 (4H, m), 4.13 (2H, m), 3.72 (1H, m), 3.55 (1H, m), 3.20 (1H, dd, J=6, 12 Hz), 1.21 (3H, t, J=6 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05428027 |
| Quelldatensatz | uspto-grants-1995_06 |
| ORD ID | ord-c5b877e7aced48708173e5628ebd3f82 |
| Quellennotiz | uspto-grants-1995_06 |