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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic acid hydrazide | HCID 1742 | — |
| Reactant | HCID 178503994 | HCID 178503994 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178515914 | HCID 178515914 | 47.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372971B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-10d2c463a0de42d781718dc460ac0b22 |
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| Source note | uspto-grants-2013_02 |
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