HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 68227143, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Reactant | 2-Amino-3-chlorobenzene-1-thiol | HCID 12678667 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68227143 | HCID 68227143 | — |
Reaction Steps
The 2-amino-3-chlorobenzenthiol (550 mg, 3.95 mmol) was dissolved in EtOH (10 mL) followed by KOH (220 mg, 3.95 mmol). To this mixture was added a solution of 1,2-dichloro-3-nitrobenzene (760 mg, 3.95 mmol) in EtOH (10 mL). The resulting reaction mixture was refluxed for 8 h to 12 h. The reaction was allowed to cool to room temperature and the residue was extracted with EtOAc and 1 mol dm−3 H3PO4. The organic layer was dried over MgSO4, filtered and evaporated to give a crude material. This crude material was purified by flash silica gel chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759336B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b98932a205814aac95f2dd6f07106339 |
| Source note | uspto-grants-2014_06 |