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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268159Generated: October 30, 2026

Acrylonitrile → HCID 14251393, compound

https://huagongshe.com/reaction/268159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
Reactant3-NitrocarbazoleHCID 76503—
CatalystBenzyltrimethylammonium hydroxideHCID 66854—
SolventBenzeneHCID 241—
ProductHCID 14251393HCID 14251393—

Reaction Conditions

Temperature50 °C

Reaction Steps

21.2 g (0.1 mol) 3-nitrocarbazole were suspended in 250 ml benzene in a three-necked flask equipped with stirrer, condenser and thermometer and present in an oil-bath, then mixed with 50 ml acrylonitrile, heated to 50°C and, after the addition of two drops of benzyl trimethyl ammonium hydroxide, reacted for two hours at 70°C, while stirring. After evaporation of the reaction mixture and recrystallization of the residue from aqueous acetone, there were obtained 22 g 9-(β-cyanoethyl)-3-nitrocarbazole, which was further worked up directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947377
Source datasetuspto-grants-1976_03
ORD IDord-30bb131a184e42c2a00676ab1349d316
Source noteuspto-grants-1976_03