HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylthiophene → HCID 700447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylthiophene | HCID 6920 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Thenoylacetonitrile | HCID 141853 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 700447 | HCID 700447 | 44% |
Reaction Steps
The procedure of Example 1 was followed except that 2-acetylthiophene (Aldrich) was used in place of acetophenone to prepare the corresponding 2-(thiophene-2-carbonyl)acetonitrile (Steps A and B). 2-Butanone (Aldrich), 2-(thiophene-2-carbonyl)acetonitrile, morpholine, and sulfur were reacted according to the procedure of Step C, Example 1, to afford the desired compound. Yield: 44%; IR (KBr) cm−1: 3390, 3269, 1552, 1429, 1272, 852, 772; 1H NMR (CDCl3):δ1.86 (s, 3H), 2.17 (s, 3H), 5.78(bs, 2H), 7.07 (dd, 1H, J=3.8 and 4.8 Hz), 7.56 (dd, 1H, J=2.8 and 0.8 Hz), 7.58 (dd, 1H, J=5.0 and 0.8 Hz); orange solid, mp: 117-118° C. (petroleum ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06727258B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-a1ed061d19634c20a617c9d45c4c12b8 |
| Source note | uspto-grants-2004_04 |