HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178432602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | 2-oxo-1,2-dihydroquinoline-4-carbaldehyde | HCID 285477 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178432602 | HCID 178432602 | — |
Reaction Steps
17 Grams of 4-formylcarbostyril, 18 g of N-acetylglycine, 7 g of anhydrous sodium acetate and 100 ml of acetic anhydride were heated at 110° C. to make a homogeneous solution, further the solution was refluxed for 1.5 hours. After cooled the reaction mixture, the reaction mixture was poured in a cold water and the crystals precipitated were collected by filtration. The crystals were washed with cold water, then recrystallized from ethanol-chloroform to obtain 10 g of 4-(1,2-dihydro-2-oxo-4-quinolyliden)-2-methyl-5-oxazolone.1/2-hydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04578381 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-cd099bf5b91543b68833e0d1c3d54b33 |
| Source note | uspto-grants-1986_03 |