HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039431Generated: October 30, 2026
Sodium t-butoxide → 9-(9-(3'-(Dibenzo[b,d]thiophen-4-yl)-[1,1'-biphenyl]-3-yl)-carbazol-3-yl)-pyrido[2,3-b]indole
https://huagongshe.com/reaction/2039431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 4-(3'-Bromobiphenyl-3-yl)dibenzothiophene | HCID 66974462 | — |
| Reactant | 9-(9H-carbazol-3-yl)-pyrido[2,3-b]indole | HCID 70815101 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Dicyclohexyl(2',6'-dimethoxybiphenyl-3-yl)phosphine | HCID 58401078 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 9-(9-(3'-(Dibenzo[b,d]thiophen-4-yl)-[1,1'-biphenyl]-3-yl)-carbazol-3-yl)-pyrido[2,3-b]indole | HCID 70815135 | 64.1% |
Reaction Steps
A solution of 9-(9H-carbazol-3-yl)-pyrido[2,3-b]indole (2.50 g, 7.50 mmol), 4-(3′-bromo-[1,1′-biphenyl]-3-yl)dibenzo[b,d]thiophene (3.11 g, 7.50 mmol), Pd2(dba)3 (0.137 g, 0.150 mmol), dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-3-yl)phosphine (0.123 g, 0.30 mmol), and sodium tert-butoxide (1.44 g, 15.00 mmol) in xylene (150 mL) was refluxed in nitrogen overnight. After cooling to room temperature, the reaction mixture was washed with water, dried over Na2SO4 and the solvent was evaporated. The residue was dissolved in hot toluene, mixed with celite, and purified by column chromatography with hexane:toluene (1:9 to 0:10, v/v) as eluent. The product was precipitated in ethanol, and further purified by thermal sublimation under vacuum (<105 torr) to yield 9-(9-(3′-(dibenzo[b,d]thiophen-4-yl)-[1,1′-biphenyl]-3-yl)-carbazol-3-yl)-pyrido[2,3-b]indole as a white glassy solid (3.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08580399B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-77d901fe3c9541b3b6d2a277e1de80e0 |
|---|
| Source note | uspto-grants-2013_11 |
|---|