HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Cyanobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyanobenzaldehyde | HCID 66042 | 30% |
| Product | HCID 43087792 | HCID 43087792 | — |
Reaction Steps
A solution of methyl 4-aminobenzoate (0.2 g, 1.323 mmol) and 4-formylbenzonitrile (0.177 g, 1.350 mmol) in methanol (2 ml) and dichloromethane (4 ml) was treated with acetic acid (0.379 ml, 6.62 mmol) followed by MP-cyanoborohydride (1.151 g, 2.65 mmol) and the reaction was slowly stirred at room temperature. After 16 hours, the mixture was filtered and concentrated and the concentrate was partitioned between 2 N sodium hydroxide and dichloromethane. The organic phase was concentrated to give the title compound with 30% of remaining 4-formylbenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193723B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-6ecaefaeab834c7cb7968d1bc9816acf |
| Source note | uspto-grants-2015_11 |