HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → 1-Fluoro-4-{2-fluoro-2-[4-(phenylsulfonyl)phenyl]ethyl}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(4-Fluorophenyl)-1-[4-(phenylsulfonyl)phenyl]ethanol | HCID 21099443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Fluoro-4-{2-fluoro-2-[4-(phenylsulfonyl)phenyl]ethyl}benzene | HCID 21099402 | — |
Reaction Steps
2-(4-Fluorophenyl)-1-[4-(phenylsulfonyl)phenyl]ethanol (Example 118, 100 mg, 0.28 mmol) was dissolved in dichloromethane (5 mL) and (diethylamino)sulfur trifluoride (0.05 mL, 0.32 mmol) added. The reaction was stirred at room temperature for 30 minutes. Saturated sodium hydrogencarbonate was added and the products extracted into ethyl acetate. The organic layer was dried over MgSO4 and evaporated. The residue was triturated with diethyl ether/isohexane to give the title compound as a beige solid. δH (360 MHz, CDCl3): 7.94-7.90 (4H, m), 7.58-7.48 (3H, m), 7.35 (2H, d, J=8.5 Hz), 7.08-7.00 (2H, m), 6.96-6.90 (2H, m), 5.69-5.53 (1H, m), 3.21-2.99 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468393B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-f73d34719b884c0b88fb0f070f7beb2b |
| Source note | uspto-grants-2008_12 |