HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → 4-[(2-Methyl-5-oxo-1,3-oxazol-4(5H)-ylidene)methyl]phenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Product | 4-[(2-Methyl-5-oxo-1,3-oxazol-4(5H)-ylidene)methyl]phenyl acetate | HCID 539527 | 89.8% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
12.2 g of 4-hydroxybenzaldehyde, 13.9 g of N-acetylglycine, 15.6 g of sodium acetate, and 51.0 g of acetic anhydride were mixed, and the mixture was stirred at 120° C. for 5 hours. After the reaction, the reaction mixture was cooled to room temperature, and 50 ml of ice-water was added thereto, followed by stirring for 1 hour. The precipitated crystals were collected by filtration and washed with 100 ml of water. The resulting crystals were vacuum dried to give 22.0 g of 4-(4-acetoxybenzylidene)-2-methyloxazol-5(4H)-one as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05684186 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-1ef52abdf0ee4f669fe18c496f462297 |
| Source note | uspto-grants-1997_11 |