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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860352Generated: October 30, 2026

Sodium Cyanide → HCID 69987899, compound

https://huagongshe.com/reaction/1860352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantHCID 69988159HCID 69988159—
ReactantHCID 178418268HCID 178418268—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 69987899HCID 6998789924.1%

Reaction Steps

0.78 g (2.00 mmol) of N-ethyl-3-(2-cyano-2-(4-trifluoromethylphenyl)ethenyl) carbazole and 10 ml of N,N-dimethylformamide as solvent were placed in a 200 ml four-necked flask with a mechanical stirrer and bulb-shaped cooler. To this was added an aqueous solution prepared from 0.10 g (2.00 mmol) of sodium cyanide and 1.0 ml of water, which was stirred for 10 minutes. Further, 0.88 g (2.00 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 solution was added 50 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 0.20 g of a yellow solid. The yield of the synthesized compound was 24%, and its melting point was 180-182° C. The IR chart is shown in FIG. 17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528657B2
Source datasetuspto-grants-2003_03
ORD IDord-6d07a612920a4b13a9df816766f17d0f
Source noteuspto-grants-2003_03