HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21520062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | HCID 21520102 | HCID 21520102 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21520062 | HCID 21520062 | — |
Reaction Steps
To a solution of 5-amino-3-ethylthio-4-phenoxybenzoic acid (1.16 g) in 1 N sodium hydroxide (4 ml), sodium nitrite (0.28 g) is added. The solution is added slowly to a mixture of acetic acid (10 ml) and concentrated hydrochloric acid (10 ml) while stirring and keeping the temperature of 2°-5°C. The resulting diazonium mixture is poured into acetic acid (20 ml), saturated with sulphur dioxide and containing copper chloride (0.2 g CuCl2, 2 H2O). The reaction mixture is allowed to reach room temperature while stirring. After cooling, the precipitated 3-ethylthio-5-chlorosulfonyl-4-phenoxybenzoic acid is collected by filtration, washed with aqueous acetic acid, and dried in vacuo at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03972886 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-2a3cacba1b4d4ecb85c0876838460e31 |
| Source note | uspto-grants-1976_08 |