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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857896Generated: November 1, 2026

p-Toluenesulfonic acid → 9,10-Dicyanoanthracene

https://huagongshe.com/reaction/1857896

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetonitrileHCID 6342—
ReactantAziridineHCID 9033—
Product9,10-DicyanoanthraceneHCID 71035—

Reaction Steps

1/5 of a 4-toluenesulfonic acid solution (PTSA H2O, 43.28 g; 0.228 mol) in CH3CN (400 mL) was added to a solution of the aziridine obtained at the previous step (229.13 g; GC 89%; 0.805 mol) and 9,10-dicyanoanthracene (DCA) (1.69 g; 7.40 mmol) in CH3CN (4.5 L). After 45 min, the remaining acid catalyst was added drop by drop to the reaction mixture in 6 hours, by means of the syringe pump. After 7.5 hours, heating and lighting were stopped. After 18 hours, water (0.5 L) and solid K2CO3 (40 g) were added with strong stirring. The organic solvent was evaporated off and the aqueous phase was extracted with CHCl3. The combined organic phases were washed with buffer 0.1M KH2PO4 /K2HPO4 at pH 7 (0.5 L), then dried over MgSO4. The crude oil resulting from the evaporation of the solvent (272.5 g) was purified by flash chromatography (CH3Cl/CH3OH/25% NH4OH (w/w) 1000:13:3 (v/v)), thereby obtaining the desired compound (51.64 g; 51.0 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06149890
Source datasetuspto-grants-2000_11
ORD IDord-82355d43687f41c0a413eb259964e31b
Source noteuspto-grants-2000_11