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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917803Generated: October 26, 2026

Toluene → 9-Phenylcarbazole

https://huagongshe.com/reaction/917803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCarbazoleHCID 6854—
ReactantBromobenzeneHCID 7961—
ReactantSodium CarbonateHCID 10340—
CatalystCuprous chlorideHCID 62652—
CatalystTetraphenylphosphonium ChlorideHCID 164911—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product9-PhenylcarbazoleHCID 70851—

Reaction Conditions

Temperature52.5 °C

Reaction Steps

Carbazole was mixed in an amount of 16.47 g (98.52 mmol) with 31.0 g (197.04 mmol) of bromobenzene, 10.44 g (98.52 mmol) of sodium carbonate, 0.4 g (8.0 mmol) of copper-(I) chloride, and 3.0 g (8.0 mmol) of tetraphenylphosphonium chloride. This mixture was reacted at 115-125° C. for 2 hours in a nitrogen stream. After the reaction, 50 mL of toluene and 100 mL of water were added and the resultant mixture was subjected to liquid separation. Thereafter, the organic layer was washed with water and dried with anhydrous sodium sulfate. After the drying agent was removed by filtration, 15.6 g of activated clay was added. The resultant mixture was stirred at 50-55° C. for 1 hour and the clay was removed by filtration. The toluene was concentrated under reduced pressure and 352 mL of methanol was added to the residue. The resultant solution was subjected to crystallization. Thus, the target compound (I-27) was obtained as white crude crystals in an amount of 22.7 g (yield, 94.8%). The target compound obtained had a melting point of 96-97° C. and a content as determined by HPLC of 99.8% (HPLC conditions: column, ODS-80TM; eluent, acetonitrile/water (V/V=65/35); buffer, triethylamine and acetic acid each in an amount of 0.1%; detection UV, 254 nm; flow rate, 1.0 mL/min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273953B2
Source datasetuspto-grants-2007_09
ORD IDord-98518565e6424e62aadd258f4d6a9b12
Source noteuspto-grants-2007_09