Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Reactant | N-nitroimidazolidin-2-imine | HCID 135413413 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136331486 | HCID 136331486 | — |
Reaction Steps
A mixture of 10.0 g of ethyl p-aminobenzoate, 10.8 g of ethyl orthoformate, 10 ml of 1,3-dimethyl-2-imidazolidinone and 0.05 g of boron trifluoride ether complex was placed in a reactor equipped with Dean's stark tube and agitated at 140° C. for about 5 minutes, followed by further addition of 7.9 g of nitroiminoimidazolidine and agitation at 180° C. for 1 hour. The reaction mixture was poured into 200 ml of a saturated saline solution, to which 150 ml of ethyl acetate was added. The resultant crystals were collected by filtration and dried to give 12.3 g of 1-(4-ethoxy-carbonylphenyliminomethyl)-2-nitroiminoimidazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05219868 |
|---|
| Source dataset | uspto-grants-1993_06 |
|---|
| ORD ID | ord-d704c87f90d0409d95b575ef0e448e32 |
|---|
| Source note | uspto-grants-1993_06 |
|---|