HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Butadiene → HCID 21292556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 5-Nitronaphthalene-1,4-dione | HCID 12336402 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21292556 | HCID 21292556 | 89% |
Reaction Steps
24.8 g of crude 5-nitronaphthoquinone (comprised of 82 wt% of 5-nitronaphthoquinone and 10 wt% of 6-nitronaphthoquinone), 12.1 g of 1,3-butadiene, and 124 g of ethanol were introduced into an autoclave. The autoclave was hermetically sealed and the reaction was effected at about 80°C for 2.5 hours. The resultant reaction solution was cooled to 25°-30°C to crystalize 5-nitrotetrahydroanthraquinone, and filtered. The cake was washed with 40 g of ethanol and dried to obtain 22.9 g of 5-nitrotetrahydroanthraquinone. The yield was 89.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959318 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-5332c618108e4c3ab5370489a08169ee |
| Source note | uspto-grants-1976_05 |