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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253321Generated: October 29, 2026

Ethanol, 1-ethoxy-2,2,2-trifluoro- → Trifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazone

https://huagongshe.com/reaction/253321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 1-ethoxy-2,2,2-trifluoro-HCID 9897—
Reactant2-Chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazineHCID 66841936—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthanolHCID 702—
ProductTrifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazoneHCID 8662893767.8%

Reaction Steps

A mixture of 4.1 g of 2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazine, 2.3 g of trifluoroacetaldehyde ethyl hemiacetal, 0.1 g of p-toluenesulfonic acid monohydrate and 50 ml of ethanol was refluxed with heating for 6 hours. The obtained reaction mixture was concentrated under reduced pressure, water was added, and the mixture was extracted with toluene. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 3.6 g of trifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872036B2
Source datasetuspto-grants-2011_01
ORD IDord-6cb27ba9bd1347ed8de689626fd87816
Source noteuspto-grants-2011_01