HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-(10-Bromoanthracen-9-yl)triphenylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(Anthracen-9-yl)triphenylene | HCID 86701357 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(10-Bromoanthracen-9-yl)triphenylene | HCID 86701358 | 88.8% |
Reaction Steps
Under the nitrogen atmosphere, 2-(anthracen-9-yl)triphenylene (3.3 g) as the eleventh intermediate compound, N-bromosuccinimide (NBS) (1.7 g), iodine (0.1 g) and THF (25 ml) were added to a flask, and stirred at room temperature for 5 hours. An aqueous solution of sodium thiosulfate was added and the reaction was terminated. The precipitates were collected by suction filtration. The obtained solid was washed with methanol and subsequently with heptane and purified by silica gel column chromatography (solvent: toluene) to give 2-(10-bromoanthracen-9-yl)triphenylene (3.5 g) as a twelfth intermediate compound. The scheme is shown in the following “Reaction 22”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09070885B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-be85ceab0e8c4df4bde8abdf2f5fa34d |
| Source note | uspto-grants-2015_06 |