HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Butadiene → HCID 69829552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | HCID 53757146 | HCID 53757146 | — |
| Catalyst | Phenothiazine | HCID 7108 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69829552 | HCID 69829552 | 125.4% |
Reaction Steps
214 g (1.0 mole) 75% 4,4-dimethoxy-1-nitro-1-butene and 0.1 g phenothiazine were put in an autoclave at room temperature, together with 850 ml toluene. Then 216 g (4.0 mole) butadiene were added under pressure. Subsequently stirring was conducted under the own pressure (approx. 6 bar) for 30 hours at 100° C. The pressure was released and the temperature reduced. Finally toluene and unreacted butadiene were distilled off. 270 g of an oily residue were obtained, containing about 39% reaction product and about 10% educt, as confirmed by GC. The crude product was employed without any further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559318B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-e1b793a1d4854bc297e42f34da47762b |
| Source note | uspto-grants-2003_05 |