HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 3002295, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | N-(2-Chloro-4-formylphenyl)acetamide | HCID 22991945 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 3002295 | HCID 3002295 | 90% |
Reaction Steps
A solution of 0.73 g (0.008 mole) of thiosemicarbazide (Aldrich T3,340-5) in 24 mL of water containing 1.6 mL of glacial acetic acid was added to a solution of 1.58 g of (0.008 mole) 4-acetamido-3-chlorobenzaldehyde (24) in 20 mL of ethanol at 700. The mixture was stirred at this temperature for 45 minutes. A white precipitate developed in the reaction mixture, which was filtered after cooling to give 1.95 g (90%) of 25 as off white crystals, mp 235-238°. Infrared (IR) and NMR analysis gave the following results:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06624153B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-33d7ea83a303449fbba95b213c4746cc |
| Source note | uspto-grants-2003_09 |