Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994017Generated: October 30, 2026

4-Hydroxybenzoic acid hydrazide → HCID 178515914, compound

https://huagongshe.com/reaction/1994017

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 numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-e32c4ef218bc436a8827321854e701ad
Source noteuspto-grants-2010_01