HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54227989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54567748 | HCID 54567748 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54227989 | HCID 54227989 | — |
Reaction Steps
11.2 g of acetic anhydride are added to a suspension of 32.4 g of 1,3-bis(pyridin-3-ylmethyleneamino)-4-hydroxy-4-methylimidazolidin-2-one in 75 ml of acetic acid. The reaction mixture is then heated to 50°. After 3 hours the reaction mixture is cooled to 20°, then poured onto 800 ml of ice-water and neutralised with 30% sodium hydroxide solution. The aqueous phase is then extracted three times with 200 ml of methylene chloride each time. The organic phase is dried with magnesium sulfate, filtered and concentrated by evaporation. The residue is stirred with ether. The crystals are filtered off with suction and dried. 28.2 g of the title compound having a melting point of 176°-178° are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783704 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-cdbb778ebec349c6a919d81c660bfb74 |
| Source note | uspto-grants-1998_07 |