HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Cyanoacetophenone → 4-[3-(3-Cyanophenyl)-1-oxo-2-propenyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Cyanoacetophenone | HCID 74044 | — |
| Reactant | m-Formylbenzonitrile | HCID 90670 | — |
| Product | 4-[3-(3-Cyanophenyl)-1-oxo-2-propenyl]benzonitrile | HCID 54499185 | — |
Reaction Steps
Part A. Employing methods similar to Example 1 Part A but using m-cyano benzaldehyde (0.91 gm, 6.89 mmol) and 4-acetyl benzonitrile (1.0 gm, 6.89 mmol), 4-[3-(3-cyanophenyl)-1-oxo-2-propenyl]benzonitrile was isolated as a pale yellow powder, 1.4 gm (79%), 1H NMR (CDCl3) 8.53(s,1H), 8.35(d,2H), 8.15-8.20(m,3H), 7.92(d, 1H), 7.82(d, 1H), 7.67(t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05942544 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-e52ee0274e43411596cc5cd44fb963d3 |
| Source note | uspto-grants-1999_08 |