HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 1-(4-Ethoxycarbonylbenzoyl)-2-cyanoaziridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Aziridine-2-carbonitrile | HCID 118115 | — |
| Reactant | Monoethyl terephthalate | HCID 164720 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Ethoxycarbonylbenzoyl)-2-cyanoaziridine | HCID 23461481 | — |
Reaction Steps
The same compound is obtained when a solution of 1.1 g. dicyclohexylcarbodiimide in 5 ml. diethyl ether is added at 0° C. to a mixture of 0.97 g. p-ethoxycarbonylbenzoic acid and 0.34 g. 2-cyanoaziridine in 15 ml. diethyl ether, stirred for 2 hours at this temperature and then for 1 hour at ambient temperature, the precipitated dicyclohexylurea is filtered off with suction (1.13 g.), the filtrate evaporated and the evaporation residue is triturated with about 3 ml. diethyl ether. The yield is 0.66 g.; m.p. 92°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04267174 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-c576984d0ea24dad9a368446f6412026 |
| Source note | uspto-grants-1981_05 |