HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 73996737, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide | HCID 2740681 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73996737 | HCID 73996737 | 59.2% |
Reaction Steps
A mixture of N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide (100 mg, 0.56 mmol), p-anisaldehyde (69 μL, 0.56 mmol) and glacial acetic acid (31 μl) in ethanol (5 mL) was stirred at room temperature for 1 h. The resultant precipitate was collected by filtration and isolated as a white solid (100 mg, 59%). 1H NMR (CDCl3): 9.05 (s, 1H), 7.72 (s, 1H), 7.57 (d, J=8.7 Hz, 2H), 7.44 (d, J=6.9 Hz, 1H), 6.93 (d, J=8.7 Hz, 2H), 6.23-6.14 (m, 2H), 4.30-4.26 (m, 1H), 3.85 (s, 3H), 3.06 (s, 1H), 2.96 (s, 1H), 1.94-1.86 (m, 1H), 1.67 (d, J=9.0 Hz, 1H), 1.51 (d, J=9.0 Hz, 1H), 1.45-1.40 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-d8c62b290db64f2684d238aa42e463a3 |
| Source note | uspto-grants-2004_09 |