Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387431Generated: October 26, 2026

4-Hydroxybenzoic acid hydrazide → HCID 178515915, compound

https://huagongshe.com/reaction/387431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic acid hydrazideHCID 1742—
Reactant1-[4-chloro-3-(trifluoromethyl)phenyl]-S-methylisothiourea hydroiodideHCID 178504001—
SolventPyridineHCID 1049—
ProductHCID 178515915HCID 17851591540.6%

Reaction Steps

4-hydroxybenzoic acid hydrazide (3.0 g, 19.66 mmol) and S-methyl N-[4-chloro-3-(trifluoromethyl)phenyl]isothiourea hydroiodide (7.8 g, 19.66 mmol) were suspended in 100 mL of anhydrous pyridine. The reaction mixture was refluxed for 18 hours under Ar atmosphere. Then it was cooled down to ambient temperature and pyridine was removed in vacuo. The resulting yellow oil was re-dissolved in a small amount of ethyl acetate, loaded on a short pad of silica gel and eluted with 5:1 hexane/ethyl acetate, then with 100% ethyl acetate to collect the product. The product was re-purified by a second silica gel column chromatography, using ISCO system (80 g pre-packed column, 25 min run, 20% to 50% EtOAc gradient in hexane). Solvent was removed in vacuo to give the title product as a white solid (2.83 g). Yield 40.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-b2e8d5a72afe43f9be9cb1b0dd3d18fb
Source noteuspto-grants-2013_02