HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 1,2-Acenaphthylenedione, 5-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acenaphthenequinone | HCID 6724 | — |
| Reactant | Bromine | HCID 24408 | — |
| Product | 1,2-Acenaphthylenedione, 5-bromo- | HCID 11173024 | — |
Reaction Steps
In the second route, the raw material acenaphthenequinone and the solvent concentrated sulfuric acid are added into liquid bromine and refluxed for 2 hours to obtain 5-bromoacenaphthylene-1,2-dione. The resulting bromoacenaphthene reacts with alcohol, thioalcohol, phenol, thiophenol, ester or amide to obtain the corresponding substituted acenaphthenequinone iv, as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08614333B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-cf298c1e08c14b6c8be08bb649eaea06 |
| Source note | uspto-grants-2013_12 |