Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178481859 | HCID 178481859 | 86.5% |
Reaction Steps
92.1 g (0.5 mole) of ethyl 4,4,4-trifluoroacetoacetate was dissolved in 60.1 g (1.0 mole) of acetic acid. The solution was cooled to 10° C. or lower with stirring. Thereto was dropwise added, in 1 hour, 65.8 g (0.5 mole) of a 35% aqueous methylhydrazine solution. After the dropwise addition, the mixture was stirred at room temperature for 1 hour and successively at 80° C. for 5 hours to give rise to a reaction. After the reaction, the mixture was cooled to room temperature. Thereto were added 150 ml of toluene, 600 ml of water and 48 g (1.2 moles) of sodium hydroxide. After phase separation, 154 g (1.5 moles) of 35% hydrochloric acid was added to the aqueous layer. The resulting crystals were collected by filtration, washed with 50 ml of water twice, and dried in a hot-air drier, to obtain 71.8 g (yield: 86.5%) of a title compound as light yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812175B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-ab2bb8514dfb4e2d97c1955190d7b886 |
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| Source note | uspto-grants-2010_10 |
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