HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hippuric Acid → HCID 53890716, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hippuric Acid | HCID 464 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20389867 | HCID 20389867 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53890716 | HCID 53890716 | — |
Reaction Steps
8.4 g (0.1 mole) of sodium bicarbonate is added, with stirring, to the mixture of 25.5 g (0.1 mole) of 5-chloro-2-(2-thienylthio)-benzaldehyde and 17.9 g (0.1 mole) of hippuric acid in 34.7 g (0.34 mole) of acetic anhydride, and the reaction mixture is stirred at 90°-95° for two hours. It is thereupon cooled to 25°; to the thick crystal mass is added 300 ml of 50% ethanol, the solid substance is filtered off with suction and is washed with 150 ml of 50% ethanol. Drying in a vacuum chamber leaves 2-phenyl-4-[5-chloro-2-(2-thienylthio)-benzylidene]-2-oxazolin-5-one in the form of yellow crystals, m.p. 125°-127°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04171366 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-a9da4f6bf4a04353abe4171d89e9bcd1 |
| Source note | uspto-grants-1979_10 |