HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzocaine → 57707-09-2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 57707-09-2 | HCID 624544 | 86.4% |
Reaction Steps
To a solution of ethyl-4-aminobenzoate (5.0 g, 30.3 mmol) in ethanol was added 2-nitrobenzaldehyde (5.03, 33.3 mmol) at room temperature. The reaction mixture was stirred at reflux for 3 h LC-MS showed ester was consumed nearly. The reaction mixture was concentrated in vacuo. The residue was washed by diethyl ether to give ethyl 4-(2-nitrobenzylideneamino)benzoate as yellow solid (7.8 g, yield 86.4%). LC/MS m/e obsd. (ESI+) [(M+H)+] 299.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546427B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ac2027e000ff4f458498a7a8685596cd |
| Source note | uspto-grants-2013_10 |