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
Ethyl 4,4,4-trifluoroacetoacetate (92.1 g (0.5 mol)) was dissolved in 60.1 g (1.0 mol) of acetic acid. The resulting solution was cooled to 10° C. or less with stirring, and 65.8 g (0.5 mol) of an aqueous 35% methylhydrazine solution was added dropwise thereto over 1 hour. After the dropwise addition, the solution was stirred at room temperature for 1 hour and subsequently at 80° C. for 5 hours. When the reaction was completed, the reaction solution was cooled to room temperature, and 150 mL (milliliter) of toluene, 600 mL of water and 48 g (1.2 mol) of sodium hydroxide were added thereto. After liquid separation, 154 g (1.5 mol) of 35% hydrochloric acid was added dropwise to the obtained aqueous layer, and the produced crystal was collected by filtration. The crystal was washed twice with 50 mL of water and dried by a hot air drier to obtain 71.8 g (yield: 86.5%) of the title compound as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488831B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-6fc8f212c5ff47d285c5be5d994579fd |
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| Source note | uspto-grants-2009_02 |
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