Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 11356278 | HCID 11356278 | — |
| Product | HCID 22677663 | HCID 22677663 | 63% |
Reaction Steps
To a solution of 2-(4-fluorophenylthio)thiophene (1.09 g, 5.18 mmol) in acetic acid (14.3 mL) was added a 30% aqueous solution of H2O2 (1.30 mL). The reaction mixture was heated at 100° C. for 45 min, then was treated with water. The resulting suspension was extracted with CH2Cl2. The combined organic layers were washed with a saturated NaHCO3 solution, dried (MgSO4) and concentrated under reduced pressure to yield 2-[(4-fluorophenyl)sulfonyl]thiophene (0.79 g, 63%) as a white solid: TLC (hex) Rf 0.08; 1H NMR (CDCl3) δ 7.09-7.27 (m, 3H), 7.67-7.71 (m, 2H), 7.99-8.04 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06784167B2 |
|---|
| Source dataset | uspto-grants-2004_08 |
|---|
| ORD ID | ord-ab82449c62cd4f96a92617fbdaf8fb12 |
|---|
| Source note | uspto-grants-2004_08 |
|---|