HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468588Generated: November 1, 2026
Ethyl trifluoroacetate → HCID 67387617, compound
https://huagongshe.com/reaction/1468588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ethyl N-phenylbenzenecarboximidothioate | HCID 13377974 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 67387617 | HCID 67387617 | 26% |
Reaction Steps
First, 1.8 g of ethyl trifluoroacetate and 50 mL of 1-butanol were put in a three-neck flask, and the air in the flask was replaced by nitrogen. After that, the mixture was stirred at 0° C. for 10 minutes, and 0.397 g of hydrazine monohydrate was dripped to the mixed solution. This mixed solution was stirred at 0° C. for 20 minutes, and then stirred at room temperature for 1 hour to be reacted. After the reaction, 3.0 g of N-[(ethylsulfanyl)phenylmethylidene]aniline was further added to the mixed solution, and the solution was heated and stirred at 120° C. for 5 hours to be reacted. The mixed solution after the reaction was cooled down to room temperature and filtered, so that filtrate was obtained. The obtained filtrate was concentrated to give a solid. This solid was washed with hexane, so that the triazole derivative HCF3ptz was prepared (yield: 26%). The synthesis scheme of Step 1 is shown by (a-2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09005773B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b70c02b5970048e48da12860c0563424 |
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| Source note | uspto-grants-2015_04 |
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