Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13561847 | HCID 13561847 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14179230 | HCID 14179230 | — |
Reaction Steps
35.4 g (0.1 mol) of 5-amino-1-(2,6-dichloro-4-trifluoromethyl-phenyl)-4-carbethoxy-pyrazole are heated under reflux for 24 hours in a solution of 8 g (0.2 mol) of sodium hydroxide, 24 ml of water and 100 ml of ethanol. 450 ml of water are subsequently added, and the mixture is washed twice with 70 ml of diethyl ether. The alcohol is removed from the aqueous phase by distillation, and 20 ml of concentrated hydrochloric acid are then added with ice cooling. The suspension is cooled to 5° C., and the precipitate is filtered off under suction, washed with water until neutral, and dried. 26.2 g (74% of theory) of the compound 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-carboxy-pyrazole of melting point 158° C. (decomposition) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04774254 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-b8182027eb3e46d6913309ed35bbf2a4 |
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| Source note | uspto-grants-1988_09 |
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