HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide → HCID 9946362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide | HCID 178 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 23505752 | HCID 23505752 | — |
| Product | HCID 9946362 | HCID 9946362 | 59.3% |
Reaction Steps
A mixture of N-[3-(2-ethyl-butyl )4,5-dimethyl-1-(2,4,6-trimethylphenyl)-1H-pyrrol-2-yl]-acetamide (100 mg, 0.27 mmol), ammonium chloride (290 mg, 5.42 mmol), and acetamide (1.635 g) was heated to reflux for 2 hours. The mixture was cooled, quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated to give 56 mg of the title compound as a dark oil. The oil was purified through silica gel column chromatography to give the title compound as a yellow oil. 1H-NMR (CDCl3) δ 0.85(t, 6H), 1.70-2.0(m, 4H), 1.83(s, 6H), 1.99(s, 3H), 2.36(s, 3H), 2.44(s, 3H), 2.61 (s, 3H), 3.26(m, 1H), 7.00(s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06765008B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-6227f7577ce044739f6294ca13461bf8 |
| Source note | uspto-grants-2004_07 |