HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → 2-Ethylthieno[2,3-b]pyridine-3-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 2-Ethylthieno[2,3-b]pyridine | HCID 12044914 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Ethylthieno[2,3-b]pyridine-3-sulfonyl chloride | HCID 12044915 | 57.3% |
Reaction Steps
To a solution of 2-ethylthieno[2,3-b]pyridine (0.43 g, 2.6 mmoles) in CH2Cl2 (10 ml) at -78° C. was added chlorosulfonic acid (0.9 ml, 13 mmoles). The reaction was warmed to ambient temperature over a 1 hr. period, then stirred an additional 20 hrs., followed by the addition of phosphorus oxychloride (1.7 ml, 18 mmoles) and phosphorus pentachloride (0.82 g, 4.0 mmoles). One hour later the reaction mixture was added to ice (100 ml) and extracted with EtOAc (75 ml), then washed with sat. NaHCO3 (200 ml). The organic phase was dried (MgSO4), filtered and concentrated to collect a brown oil. Flash chromatography (10% EtOAc/hexanes) provided 0.39g (56%) of the title compound as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05804585 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-af930e140a5746a788f9c9f5407c6e44 |
| Source note | uspto-grants-1998_09 |