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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387464Generated: October 26, 2026

4-Chloro-3-trifluoromethylbenzoic acid hydrazide → HCID 178516245, compound

https://huagongshe.com/reaction/387464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-trifluoromethylbenzoic acid hydrazideHCID 21311701—
ReactantHCID 178504017HCID 178504017—
SolventPyridineHCID 1049—
ProductHCID 178516245HCID 17851624545.5%

Reaction Steps

4-chloro-3-trifluoromethylbenzoic acid hydrazide (2.89 g, 12.1 mmol) and S-methyl N-(4-hydroxyphenyl)isothiourea hydroiodide (3.75 g, 12.1 mmol) were suspended in 40 mL of anhydrous pyridine. The reaction mixture was refluxed for 18 hours, during which time it changed color from yellow into dark-red. Then it was cooled down to ambient temperature and poured with stirring into 250 mL of ice-water. The aqueous solution was decanted and the oily 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 white solid (1.95 g). Yield 45.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-29f58fadcc4f4fffaf799caa5f7ebbc1
Source noteuspto-grants-2013_02