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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387445Generated: October 27, 2026

4-Hydroxybenzoic acid hydrazide → HCID 178515914, compound

https://huagongshe.com/reaction/387445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic acid hydrazideHCID 1742—
ReactantHCID 178503994HCID 178503994—
SolventPyridineHCID 1049—
ProductHCID 178515914HCID 17851591447.6%

Reaction Steps

S-methyl N-[3-(trifluoromethyl)phenyl]isothiourea hydroiodide (9.09 g, 25.11 mmol) and 4-hydroxybenzoic acid hydrazide (3.82 g, 25.11 mmol) were suspended in ca. 50 mL of anhydrous pyridine under Ar. The mixture was brought to reflux and refluxed under Ar for 12 hrs. Then the dark-yellow solution was cooled down to ambient temperature and pyridine was removed in vacuo. The resulting reddish-yellow solid was re-dissolved in ca. 50 mL of 4:1 mixture of EtOAc/MeOH, ca. 20 g of silica gel was added and solvent was removed in vacuo. The impregnated silica gel was loaded into 25 g ISCO sample cartridge and the product was purified using ISCO system (solid method, 80 g column, 45 min, 0% to 50% EtOAc gradient in hexane). Solvent was removed in vacuo to give the title product as a white solid (3.83 g). Yield 47.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-10d2c463a0de42d781718dc460ac0b22
Source noteuspto-grants-2013_02