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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283157Generated: October 31, 2026

Carbazole → 1-Phenyl-9H-carbazole

https://huagongshe.com/reaction/2283157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantIodobenzeneHCID 11575—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product1-Phenyl-9H-carbazoleHCID 1349747484.1%

Reaction Steps

Ina stream of argon, 670 g of carbazole, 850 kg of iodobenzene, 20 L of xylene, 460 g of t-BuONa, and palladium acetate (Pd(OAc)2) were added, and then the mixture was refluxed for 8 hours. Impurities were filtrated, and then the filtrate was concentrated under reduced pressure and washed with hexane. After that, the washed product was dried. As a result, 820 g of phenylcarbazole were obtained as a white powder. In a stream of argon, 24 g of phenylcarbazole, 8.3 g of potassium iodide, 10.7 g of potassium iodate, 500 mL of ethanol, and 8 mL of sulfuric acid were added into a 1,000-mL three-necked flask, and then the mixture was stirred at 75° C. for 2 hours. After that, the reaction product was injected into ice water, and then the mixture was extracted with ethyl acetate and water. After having been washed with water, the extract was subjected to column chromatography with silica gel. As a result, 67 g of a white powder were obtained. A reaction was performed in the same manner as in the synthesis of Intermediate 1 except that 9-phenylcarbazole was used instead of 4-bromobiphenyl. As a result, 22.3 g of a white powder were obtained. FD-MS analysis identified the powder as Intermediate 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145363B2
Source datasetuspto-grants-2015_09
ORD IDord-0621cbca20fe413b8259af4cea26ecef
Source noteuspto-grants-2015_09