Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Furan | HCID 8029 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Product | Furan-2-sulfonyl Chloride | HCID 2795072 | 8.3% |
Reaction Steps
Phosphorus pentachloride (15.29 g, 73.44 mmol) was added portionwise (caution, foaming) over 5 min at 0° C. to chlorosulfonic acid (21.39 g, 183.6 mmol) and the resulting solution was stirred at 0° C. for 10 min. Then, furan (5.0 g, 73.44 mmol) was added in one portion and the resulting dark suspension was stirred at 0° C. for 15 min during which time foaming occurred and subsided. The reaction mixture was then poured onto ice and the resulting suspension was extracted with CH2Cl2 (150 mL). The organic extract was filtered through a pad of celite, washed with brine and dried over MgSO4. The solvent was removed in vacuo to provide 2-furansulfonyl chloride as a black oil (1.01 g, 7.9%). 1H-NMR (DMSO-d6, 400 MHz) δ 7.4 (d, 1H); 6.38 (d, 1H); 6.35 (d, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07691884B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-733173ecfc8f4ccb9bd4030d606d20f4 |
|---|
| Source note | uspto-grants-2010_04 |
|---|