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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661406Generated: October 25, 2026

4-(Trifluoromethoxy)benzoic acid hydrazide → HCID 178516246, compound

https://huagongshe.com/reaction/661406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)benzoic acid hydrazideHCID 2777230—
ReactantHCID 178504017HCID 178504017—
SolventPyridineHCID 1049—
ProductHCID 178516246HCID 17851624640.7%

Reaction Steps

4-trifluoromethoxybenzoic acid hydrazide (1.1 g, 5.0 mmol) and S-methyl N-[4-hydroxy-phenyl]isothiourea hydroiodide (1.55 g, 5.0 mmol) were suspended in 10 mL of anhydrous pyridine. The reaction mixture was refluxed for 24 hours, during which time it changed color from yellow into orange-red. Then it was cooled down to ambient temperature and poured with stirring into 150 mL of ice-water. The aqueous layer was decanted and the resulting residue was purified by silica gel chromatography using 1:1 mixture of ethyl acetate/hexane. Solvent was removed in vacuo to give the title product as a pinkish-grey solid (684.0 mg). 40.6% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084618B2
Source datasetuspto-grants-2011_12
ORD IDord-2056e679c251450483be3557ce791971
Source noteuspto-grants-2011_12