HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonylhydrazide → HCID 178427625, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Reactant | 2-[(Dimethylamino)methylidene]cyclohexane-1,3-dione | HCID 359353 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178427625 | HCID 178427625 | 100% |
Reaction Steps
According to Scheme 3 Step 1: 4-Methylbenzenesulfonohydrazide (44.6 mmol, 8.31 g) was added to a solution of 2-((dimethylamino)methylene)cyclohexane-1,3-dione (44.6 mmol, 7.46 g) in EtOH (50 mL) and the reaction mixture was stirred at room temperature for 5 minutes. After evaporation, 13.8 g (44.6 mmol, 100%) of N′-((2,6-dioxocyclohexylidene)methyl)-4-methylbenzenesulfonohydrazide were obtained as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697744B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-ce0c360e71c14c04b674cf862caf49ed |
| Source note | uspto-grants-2014_04 |