HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aziridine-2-carbonitrile → HCID 21161967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aziridine-2-carbonitrile | HCID 118115 | — |
| Reactant | 1,3-benzodioxole-5-carboxamide | HCID 230365 | — |
| Reactant | HCID 21202813 | HCID 21202813 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21161967 | HCID 21161967 | — |
Reaction Conditions
| Temperature | 0 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282212 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-e1c7266a4dcb413680d5f1d2fdc9776f |
| Source note | uspto-grants-1981_08 |