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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893964Generated: October 30, 2026

Aziridine-2-carbonitrile → HCID 21161967, compound

https://huagongshe.com/reaction/893964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridine-2-carbonitrileHCID 118115—
Reactant1,3-benzodioxole-5-carboxamideHCID 230365—
ReactantHCID 21202813HCID 21202813—
SolventTolueneHCID 1140—
ProductHCID 21161967HCID 21161967—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.26 g. 2-Cyanoaziridine are dissolved in 5 ml. toluene and introduced, while stirring at 0° C., into a solution of 0.73 g. 3,4-methylenedioxybenzoyl isocyanate in 25 ml. toluene. The reaction mixture is further stirred for 1 hour at 0° C. and the precipitated material (0.65 g.) is filtered off with suction at ambient temperature and briefly boiled with isopropanol, 0.2 g. of the desired 1-(N-3,4-methylenedioxybenzoyl-carbamoyl)-2-cyanoaziridine thereby remaining undissolved (m.p. 145°-153° C., at 172° C. a clear melt is obtained). It is contaminated with a little 3,4-methylenedioxybenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282212
Source datasetuspto-grants-1981_08
ORD IDord-e1c7266a4dcb413680d5f1d2fdc9776f
Source noteuspto-grants-1981_08