Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 11773086 | HCID 11773086 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 16040978 | HCID 16040978 | — |
Reaction Steps
5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4,5-dihydro-pyrazole-3-carboxylic acid (0.55 g, 1.50 mmol) was dissolved in 20 mL of toluene and (2 mL) ethanol and (0.05 g) of p-toluenesulfonic acid monohydrate were added. The mixture was heated at 80° C. for 72 hours. After cooling to room temperature, the reaction mixture washed with sodium hydrogen carbonate solution and water, dried over sodium sulphate and evaporated to dryness to give the title compound in form of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207156B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-7a774b1eefa745a9b7734f69f92248ea |
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| Source note | uspto-grants-2012_06 |
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