HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 15337398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | 4-(Methylthio)benzaldehyde | HCID 76985 | — |
| Reactant | HCID 11197095 | HCID 11197095 | — |
| Solvent | Acetic acid toluene | HCID 18331056 | — |
| Product | HCID 15337398 | HCID 15337398 | — |
Reaction Steps
To phenylhydrazine (50 uL) in toluene-HOAc (2:1, 2 mL) was added 2-(4-fluorophenyl)-1-(4-(methylsulfonyl)phenyl)ethanone (105 mg) (prepared from 4-(methylthio)benzaldehyde and 4-fluorobenzyl chloride by the same method as described in Step 1 of Example 4). After 1 hr at 85° C., the reaction mixture was extracted with EtOAc and HCl. After drying over NaSO4 and evaporation in vacuo the title compound was purified by flash chromatography (67 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521213 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-7a007ac9cdab40358cecf633ee5e1d0e |
| Source note | uspto-grants-1996_05 |