HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → HCID 178481951, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | HCID 19779905 | HCID 19779905 | — |
| Reactant | HCID 178516149 | HCID 178516149 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178481951 | HCID 178481951 | — |
Reaction Steps
Another method of making 5-trifluoromethyl-3-hydroxypyrazole involves reacting the ethyl 4,4,4-trifluoroacetoacetate directly with the methylhydrazine in ether to form a mixture of the intermediates 5-hydroxypyrazolidin-3-one and 3-hydroxypyrazolidin-5-one and dehydration of these intermediates by the addition of sulfuric acid in chloroform to form a mixture of the 3- and 5-hydoxypyrazoles. The desired isomer can be separated as described above. Alternatively, 2,4,4 trifluoroacetoacetate can be reacted in a like manner to give 1-methyl-3-hydroxy-4-fluoro-5-difluoromethylpyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855442 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-f969f7d916a0457b93d75b0beb8cff60 |
| Source note | uspto-grants-1989_08 |