HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 10425502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Dichromate ion | HCID 24503 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10807217 | HCID 10807217 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10425502 | HCID 10425502 | — |
Reaction Steps
The title compound was prepared from 1-(4-methyl-phenacyl)-quinolinium bromide (120 mg, 0.350 mmol), tetrapyridinecobalt(II) dichromate (229 mg, 0.376 mmol), sodium bicarbonate (74.7 mg, 0.889 mmol), acrylonitrile (120 μL, 1.82 mmol), and N,N-dimethylformamide (2.5 mL), similar to Example 1b, and yielded 30.6 mg (28%) as a yellow solid. 1H NMR (CDCl3): 8.05 (d, J=8.51 Hz, 1H), 7.98 (dd, J=6.60, 1.65 Hz, 2H), 7.84 (dd, J=7.83, 1.51 Hz, 1H), 7.71 (d, J=9.34 Hz, 1H), 7.67 (d, J=9.07 Hz, 1H), 7.60 (ddd, J=8.24, 7.08, 1.58 Hz, 1H), 7.52 (td, J=7.49, 1.19 Hz, 1H), 7.40 (s, 1H), 7.37 (d, J=7.97 Hz, 2H), 2.50 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135480B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-12f61d025f934338ae84fa864fa497da |
| Source note | uspto-grants-2006_11 |