HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorothiophenol → Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorothiophenol | HCID 520216 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-(4-fluorophenyl)acrylate | HCID 19736751 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate | HCID 19927552 | 82.2% |
Reaction Steps
The crude product from Step A (3.9 g, 20 mmole) 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05182303 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-ae3ef02d26014c06b8231c688f6a2538 |
| Source note | uspto-grants-1993_01 |