HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromobenzene → 1,4-Bis(anthracen-9-yl)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromobenzene | HCID 11414 | — |
| Reactant | 1,4-Dibromonaphthalene | HCID 66521 | — |
| Reactant | 9-Anthraceneboronic Acid | HCID 15510213 | — |
| Product | 1,4-Bis(anthracen-9-yl)naphthalene | HCID 59133425 | — |
Reaction Steps
Procedure analogous to Example 3a. Instead of 149.0 ml (1.2 mol) of 1,2-dibromobenzene and 98.0 g (308 mmol) of 9,10-anthracenediboronic acid ethylene glycol ester, 28.6 g (100 mmol) of 1,4-dibromonaphthalene and 68.0 g (306 mmol) of 9-anthraceneboronic acid are used. After cooling, the solid is filtered off with suction and washed twice with 500 ml of boiling ethanol each time. Yield: 33.0 g (69 mmol), 68.7% of theory; purity: 98% according to 1H-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08674141B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-7f37cb8c35414d9daf1baae32eec3e51 |
| Source note | uspto-grants-2014_03 |