HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 10022323, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Dichromate ion | HCID 24503 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21892166 | HCID 21892166 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10022323 | HCID 10022323 | — |
Reaction Steps
The title compound was prepared from 1-(3-bromo-phenacyl)-quinolinium bromide (150 mg, 0.368 mmol), tetrapyridinecobalt(II) dichromate (306 mg, 0.502 mmol), sodium bicarbonate (96.3 mg, 1.15 mmol), acrylonitrile (150 μL, 2.28 mmol), and N,N-dimethylformamide (4.0 mL), similar to Example 1b, and yielded 21.2 mg (15%) as a yellow solid. 1H NMR (CDCl3): 8.20 (t, J=1.79 Hz, 1H), 8.06 (d, J=8.51 Hz, 1H), 7.98 (dt, J=6.25, 1.38 Hz, 1H), 7.86 (dd, J=7.83, 1.51 Hz, 1H), 7.81 (ddd, J=6.52, 2.06, 0.96 Hz, 1H), 7.76 (d, J=9.06 Hz, 1H), 7.69 (d, J=9.06 Hz, 1H), 7.63 (ddd, J=8.31, 7.14, 1.65 Hz, 1H), 7.56 (td, J=7.41, 1.10 Hz, 1H), 7.45 (t, J=7.83 Hz, 1H), 7.44 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135480B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-54fc46efc60d4d139327102eb6e7964c |
| Source note | uspto-grants-2006_11 |