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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium t-butoxideHCID 23676156—
Reactant4-(3'-Bromobiphenyl-3-yl)dibenzothiopheneHCID 66974462—
Reactant9-(9H-carbazol-3-yl)-pyrido[2,3-b]indoleHCID 70815101—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystDicyclohexyl(2',6'-dimethoxybiphenyl-3-yl)phosphineHCID 58401078—
SolventO-XyleneHCID 7237—
Product9-(9-(3'-(Dibenzo[b,d]thiophen-4-yl)-[1,1'-biphenyl]-3-yl)-carbazol-3-yl)-pyrido[2,3-b]indoleHCID 7081513564.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580399B2
Source datasetuspto-grants-2013_11
ORD IDord-77d901fe3c9541b3b6d2a277e1de80e0
Source noteuspto-grants-2013_11