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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860351Generated: October 27, 2026

Sodium Cyanide → N-(4-methoxyphenyl)-3-(tricyanoethenyl)carbazole

https://huagongshe.com/reaction/1860351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantN-(4-methoxyphenyl)-3-(2,2-dicyanoethenyl)carbazoleHCID 18627171—
ReactantHCID 178418268HCID 178418268—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductN-(4-methoxyphenyl)-3-(tricyanoethenyl)carbazoleHCID 1862719527.9%

Reaction Steps

1.00 g (2.87 mmol) of N-(4-methoxyphenyl)-3-(2,2-dicyanoethenyl)carbazole and 12.5 ml of N,N-dimethylformamide as solvent were placed in a 500 ml four-necked flask with a mechanical stirrer and bulb-shaped cooler. To this was added an aqueous solution prepared from 0.15 g (2.87 mmol) of sodium cyanide and 0.5 ml of water, which was stirred for 10 minutes. Further, 1.74 g (3.93 mmol) of lead tetraacetate was added. The resultant product was subjected to the reaction for 30 minutes. After the reaction was completed, 100 ml of chloroform was added. To the resultant aqueous solution was added 100 ml of water. The resultant liquid was washed in a separatory funnel. To the washed liquid was added sodium sulfate, which was left to stand for 30 minutes and dehydrated. The dehydrated solution was concentrated in an evaporator and dried under vacuum to obtain a red solid, which was recrystallized in the presence of benzene to obtain 0.30 g of a red crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528657B2
Source datasetuspto-grants-2003_03
ORD IDord-314515197ce14e4ba1e439436be62514
Source noteuspto-grants-2003_03