HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 13106290, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13564370 | HCID 13564370 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13106290 | HCID 13106290 | 84.8% |
Reaction Steps
In 1,000 ml of acetonitrile was suspended 17 g of 5-{2-[2-(2-ethoxyphenoxy)ethylamino]-1-hydroxy-2-methylethyl}-2-methoxybenzenesulfonamide hydrochloride and while stirring the suspension, 9 g of thionyl chloride was added dropwise to the suspension at room temperature, whereby the product first dissolved and then began to crystallize gradually. After stirring the mixture for two days, the crystals formed were recovered by filtration, washed with chloroform and dried to provide 15 g of 5-{1-chloro-2-[2-(2-ethoxyphenoxy)ethylamino]-2-methylethyl}-2-methoxybenzenesulfonamide hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761500 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-d9175dfda47143f4bd849e239a7e1c75 |
| Source note | uspto-grants-1988_08 |