HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028870Generated: October 25, 2026
Tris(1,1-dimethylethyl)phosphine → 9-(4-[Benzoxazol-2-yl)phenyl]-3,6-diphenyl-9H-carbazole
https://huagongshe.com/reaction/1028870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | 3,6-Diphenylcarbazole | HCID 3123295 | — |
| Reactant | 2-(4-Bromophenyl)benzo(d)oxazole | HCID 12846715 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 9-(4-[Benzoxazol-2-yl)phenyl]-3,6-diphenyl-9H-carbazole | HCID 58281799 | — |
Reaction Steps
In a 100 mL three-neck flask were put 1.0 g (3.7 mmol) of 2-(4-bromophenyl)benzoxazole, 1.2 g (3.7 mmol) of 3,6-diphenyl-9H-carbazole, and 0.77 g (8.0 mmol) of sodium tert-butoxide. The atmosphere in the flask was replaced with nitrogen. To this mixture were added 15 mL of toluene and 0.10 mL of a 10% hexane solution of tri(tert-butyl)phosphine. This mixture was degassed by reducing the pressure in the flask by using an aspirator. After that, the atmosphere in the flask was replaced with nitrogen. To this mixture was added 0.030 g (0.052 mmol) of bis (dibenzylideneacetone)palladium(0), followed by stirring under a nitrogen stream at 80° C. for 5 hours. After that, toluene was added to this mixture, and this suspension was suction filtered through Celite 545 (produced by Kishida Chemical Co., Ltd., Catalog No. 020-14815), whereby a filtrate was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735597B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b67aa0056f514279bad981628d21f93c |
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| Source note | uspto-grants-2014_05 |
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