HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5-[(2-Methoxyphenyl)methylene]-2-thioxo-4-imidazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Thiohydantoin | HCID 1274030 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[(2-Methoxyphenyl)methylene]-2-thioxo-4-imidazolidinone | HCID 3004672 | 85.4% |
Reaction Steps
A mixture of 2-methoxybenzaldehyde (2.5 g, 18 mmoles), 2-thiohydantoin (2.0 g, 17 mmoles), sodium acetate (4.0 g, 49 mmoles), acetic anhydride (μml), and acetic acid (15 ml) is stirred under an inert atmosphere and heated to reflux. After 1 hour the mixture is stirred into water (300 ml), and the precipitate is filtered off, rinsed with water three times and dried. The product is triturated in boiling methanol, filtered off, and dried to afford the pure product (3.4 g), mp 234°-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464856 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-c994d1b65e984355a391b6af2b305182 |
| Source note | uspto-grants-1995_11 |