HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonylhydrazide → 11beta-Methoxy-17-tosylhydrazono-estra-1,3,5(10)-trien-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Reactant | 11beta-Methoxy-3-hydroxy-estra-1,3,5(10)-trien-17-one | HCID 11208813 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 11beta-Methoxy-17-tosylhydrazono-estra-1,3,5(10)-trien-3-ol | HCID 69529465 | — |
Reaction Steps
In a mixture of 6 ml of ethanol and 4 ml of glacial acetic acid, 1 g (3.3 mmol) of 3-hydroxy-11β-methoxy-estra-1,3,5(10)-trien-17-one and 0.7 g (3.8 mmol) of toluene-4-sulfonic acid hydrazide are refluxed. After a reaction time of about 5 hours at boiling heat, the reaction mixture is cooled, and the product is isolated in about 100 ml of water by addition in drops. By boiling the crude product in n-hexane, the water that is contained is azeotropically removed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109360B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-553214bdfaff459c866558982e8d0862 |
| Source note | uspto-grants-2006_09 |