HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Indandione → HCID 178464434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Reactant | HCID 178464435 | HCID 178464435 | — |
| Product | HCID 178464434 | HCID 178464434 | — |
Reaction Steps
3.5 g (10.33 mmol) 4-chloro-2-((E)-{4-[ethyl(2-hydroxyethyl)amino]phenyl}-diazenyl)-1,3-thiazole-5-carbaldehyde and 2.33 g (15.50 mmol) 1H-indene-1,3(2H)-dione were dissolved in 90 ml ethanole and stirred under reflux. After 6 hours the mixture was allowed to cool to room temperature. The formed precipitate was filtered, washed with ethanol and dried in vacuum at 40° C. to obtain a dark powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977482B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-ed59b666fad641eeae51fa2b47773487 |
| Source note | uspto-grants-2011_07 |