HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(Acetyloxy)-3,5-dichlorobenzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 3,5-Dichloro-2-hydroxybenzenesulphonyl chloride | HCID 90078 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Acetyloxy)-3,5-dichlorobenzenesulfonyl chloride | HCID 18981627 | — |
Reaction Steps
A pyridine solution (1.1 g of pyridine in 10 ml of methylene chloride) was added dropwise over 30 minutes to a solution of 3.37 g of 3,5-dichloro-2-hydroxybenzenesulfonyl chloride, 25 ml of methylene chloride and 1.1 g of acetyl chloride. After two hours of stirring at room temperature the starting sulfonyl chloride was no longer present and one major product had formed. The reaction was concentrated and used immediately.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05272128 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-49bad14d86af4428b7bf8cbc470e0027 |
| Source note | uspto-grants-1993_12 |