HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-[(2,5-Dioxoimidazolidin-4-ylidene)methyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[(2,5-Dioxoimidazolidin-4-ylidene)methyl]benzonitrile | HCID 54142030 | — |
Reaction Steps
36.7 g (0.28 mol) of 4-cyanobenzaldehyde, 10 g (0.1 mol) of hydantoin, 21.6 g (0.263 mol) of sodium acetate and 28.6 ml (0.3 mol) of acetic anhydride are heated under reflux in 85 ml of acetic acid for 4 hours. After cooling, the mixture is poured onto ice and extracted with methylene chloride. The methylene chloride phase is concentrated, and the residue is stirred with methanol and filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389614 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-afeed6daf91b4b52bfee03ef4c2b5346 |
| Source note | uspto-grants-1995_02 |