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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860354Generated: November 4, 2026

Sodium Cyanide → HCID 73454077, compound

https://huagongshe.com/reaction/1860354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantHCID 73454080HCID 73454080—
ReactantHCID 178418268HCID 178418268—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 73454077HCID 7345407719.2%

Reaction Steps

0.50 g (0.93 mmol) of N-(4-methoxyphenyl)-3-(2-cyano-2-(3,5-bis(trifluoromethyl) phenyl)ethenyl)carbazole and 5 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 0.05 g (1.00 mmol) of sodium cyanide and 0.5 ml of water, which was stirred for 10 minutes. Further, 0.44 g (1.00 mmol) of lead tetraacetate was added. The resultant product was subjected to the reaction for 30 minutes. After the reaction was completed, 20 ml of chloroform was added. To the resultant solution was added 20 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 vermilion solid. The vermilion solid was recrystallized in the presence of ethanol to obtain 0.10 g of an orange crystal. The yield of the synthesized orange crystal was 19%, and its melting point was 170-172° C. The IR chart is shown in FIG. 21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528657B2
Source datasetuspto-grants-2003_03
ORD IDord-a8956bd4849646afb874b32ff3fbe522
Source noteuspto-grants-2003_03