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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659613Generated: October 30, 2026

Carbazole → N-Benzylcarbazole

https://huagongshe.com/reaction/659613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductN-BenzylcarbazoleHCID 14648590.3%

Reaction Steps

A 100-mL round-bottomed flask was charged with a solution of 9H-carbazole (1.67 g, 9.90 mmol, 1.00 equiv, 99%) in DMF (20 mL) followed by addition of NaH (400 mg, 16.50 mmol, 1.00 equiv, 99%) in small portions at 0° C. over 5 minutes. 1-(Bromomethyl)benzene (1.7 g, 9.90 mmol, 1.00 equiv, 99%) was then added drop wise at 0° C. over 5 minutes. The resulting mixture was stirred at room temperature for 16 hours. The progress was monitored by TLC (EtOAc:PE=1:5). Upon completion, the reaction was then quenched by the addition of water/ice (100 mL). The solids were collected by filtration and dried in an oven under reduced pressure to afford 9-benzyl-9H-carbazole as white solid (2.3 g, 90%). LCMS: [M+H]+: 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080566B1
Source datasetuspto-grants-2011_12
ORD IDord-c58f6de1c7b3428f9031ff6318a9c828
Source noteuspto-grants-2011_12