HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5-[(2-Methoxyphenyl)methylene]-3-methyl-2,4-imidazolidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | 2,4-Imidazolidinedione, 3-methyl- | HCID 138851 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[(2-Methoxyphenyl)methylene]-3-methyl-2,4-imidazolidinedione | HCID 54177041 | 63.6% |
Reaction Steps
A mixture of 2-methoxybenzaldehyde (3.4 g,25 mmoles), 3-methyl hydantoin (3.0 g, 21 mmoles), sodium acetate (6.0 g, 73 mmoles), acetic anhydride (3 ml), and acetic acid (20 ml) is stirred under an inert atmosphere and heated to reflux. After 15 hours the mixture is poured into water (200 ml), stirred, and the precipitate filtered off, rinsed three times with water and dried. Recrystallization from acetonitrile gave the pure product (3.1 g), mp 189°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05208250 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-d4fcc92c23f14244a83c75c92919786a |
| Source note | uspto-grants-1993_05 |