HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-[(4-Chlorobenzyl)amino]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-[(4-Chlorobenzyl)amino]benzoic acid | HCID 3975397 | 78% |
Reaction Steps
4-Aminobenzoic acid (13.7 g., 0.1 mole) and 4-chlorobenzaldehyde (14.05 g., 0.1 mole) were mixed in dry benzene (200 ml.), 4-toluenesulphonic acid (50 mg.) was added and the mixture was boiled under reflux in an apparatus incorporating a water-trap until the theoretical amount of water (1.8 ml) had been collected. The reaction mixture was cooled in iced water, the product filtered, dried and hydrogenated at NTP in ethanol (500 ml) in the presence of platinum oxide, (Adams catalyst), (100 mg). The catalyst was filtered off and the solution added to iced water. The product was filtered, dried and crystallised from 20% aqueous ethanol to give 4[(4-chlorobenzyl)-amino]-benzoic acid (17.32 g., 78%) which melted at 206°-8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04206145 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-0338624c85294097b7a1e08ab8ce6936 |
| Source note | uspto-grants-1980_06 |