HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 20556953, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | HCID 178458361 | HCID 178458361 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20556953 | HCID 20556953 | — |
Reaction Steps
34 g of 3-{5-[2-(2,4-di-tert-amylphenoxy)butyramido]-2-chloroanilino}-1-(2,4,6-trichlorophenyl)-4-(1-pyrazolyl)-5-oxo-2-pyrazoline (prepared by the method described in German Patent Application (OLS) No. 2,536,191), 25 g of isopropenyl acetate and 0.5 g of p-toluenesulfonic acid were added to 250 ml of benzene and the mixture was refluxed for 5 hours. After the reaction, the reaction mixture was condensated under reduced pressure. Upon crystallization of the residue from a solvent mixture of benzene and hexane, 23 g of Coupler (2) was obtained. The melting point of the coupler was 102° to 108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308343 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-1e5ad509d49746acbf7666956e20e430 |
| Source note | uspto-grants-1981_12 |