HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 131733676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | HCID 12752104 | HCID 12752104 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131733676 | HCID 131733676 | — |
Reaction Steps
A mixture of (4,5,6,7-tetrachlorobenzo[d][1,3]dioxol-2-yl)(thiophen-2-yl)methanone (1 g, 2.70 mmol) and phenyl hydrazine (880 mg, 8.13 mmol) in ethanol (14 mL) was heated under reflux for 30 minutes. The reaction mixture was then cooled in an ice bath. A solid precipitated, and the precipitate was collected by filtration and washed with hexane. Crude 2,2′-(1-(thiophen-2-yl)ethane-1,2-diylidene)bis(1-phenylhydrazine) was obtained as a brown solid (500 mg, 57.8% yield) and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09173401B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-0516f1e417c84e7fa01b74f129b935bf |
| Source note | uspto-grants-2015_11 |