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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468588Generated: November 1, 2026

Ethyl trifluoroacetate → HCID 67387617, compound

https://huagongshe.com/reaction/1468588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantEthyl N-phenylbenzenecarboximidothioateHCID 13377974—
Solvent1-ButanolHCID 263—
ProductHCID 67387617HCID 6738761726%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09005773B2
Source datasetuspto-grants-2015_04
ORD IDord-b70c02b5970048e48da12860c0563424
Source noteuspto-grants-2015_04