HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → HCID 67134284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | HCID 67134126 | HCID 67134126 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67134284 | HCID 67134284 | — |
Reaction Steps
3.24 g (60 mmol) of butadiene were condensed at −78° C. into an autoclave under a nitrogen atmosphere. 2.03 g (10 mmol) of 3,4,5-trifluoro-β-nitrostyrene from example 2.2 dissolved in 6 ml of toluene and 30 mg of hydroquinone were added. A nitrogen atmosphere was applied (120 bar) and the suspension was heated for 12 h to 130° C. The reaction mixture was expanded and all volatiles were evaporated in vacuo. Column chromatography (SiO2, cyclohexane/ethylacetate 9:1) yielded 2.4 g (9.4 mmol, 94% of theory) of the title compound as yellowish crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853455B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-a7d5502a7a9247db83f59d688307b443 |
| Source note | uspto-grants-2014_10 |