HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Allyl-4-hydroxybenzaldehyde | HCID 4729014 | — |
| Product | 2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazolone | HCID 53677355 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
40.5 g (0.25 mol) of 3-allyl-4-hydroxy-benzaldehyde, 10.3 g of sodium acetate, 19.9 g of N-acetylglycine and 63.5 g of acetic anhydride are together heated for 30 minutes to 100°C and then for 21/2 hours to the reflux temperature. The resulting solution is cooled to 0°C and the crystals which have separated out are filtered off, washed with water, dried in a vacuum desiccator and finally recrystallised from carbon tetrachloride. 2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazolone of melting point 108°-109°C is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014920 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-97f9d10739114340918dadef831fe861 |
| Source note | uspto-grants-1977_03 |