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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387451Generated: October 26, 2026

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

https://huagongshe.com/reaction/387451

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 numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-b6dbb7ea7e3445c9bd39fbadf17acb60
Source noteuspto-grants-2013_02