HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 20089846, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | HCID 568432 | HCID 568432 | — |
| Reactant | 7,8-Dibromobicyclo[4.2.0]octa-1,3,5-triene | HCID 568434 | — |
| Reactant | HCID 20059337 | HCID 20059337 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20089846 | HCID 20089846 | — |
Reaction Steps
25 mmol of 6,7-bis-trifluoromethyl-1,4-naphthquinone, approx. 37 mmol of 1,2-dibromobenzocyclobutene [see J. Am. Chem. Soc. 79, pages 1701 et seq. (1957)] containing a little 1-bromo-2-iodobenzocyclobutene and 100 ml of xylene are kept under reflux for 16 hours in a water separator. The reaction mixture is cooled and the precipitate is filtered off and washed with xylene. The crystalline 2,3-di-(trifluoromethyl)-naphthacene-5,12-dione is obtained in a yield of 5.82 g (71%), melting point>280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05011944 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-46a93b17d6a64a4e8bf486c845bf92a7 |
| Source note | uspto-grants-1991_04 |