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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706041Generated: October 31, 2026

Water → 4-[(4-Chlorobenzyl)amino]benzoic acid

https://huagongshe.com/reaction/1706041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Aminobenzoic AcidHCID 978—
Reactant4-ChlorobenzaldehydeHCID 7726—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product4-[(4-Chlorobenzyl)amino]benzoic acidHCID 397539778%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206145
Source datasetuspto-grants-1980_06
ORD IDord-0338624c85294097b7a1e08ab8ce6936
Source noteuspto-grants-1980_06