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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266027Generated: November 1, 2026

Acetonitrile → 4-Aminobenzoic Acid

https://huagongshe.com/reaction/266027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantN-Trichloroacryloyl-p-aminobenzoic acidHCID 19032249—
SolventMethanolHCID 887—
Product4-Aminobenzoic AcidHCID 978—

Reaction Steps

N-Trichloroacryloyl-p-aminobenzoic acid (440 μg) was dissolved in 1 mL of methanol, and 100 μL of this solution was added to 300 μL of potassium phosphate buffer (0.1 M, pH 8). In the same way a solution of p-aminobenzoic acid was prepared. Both solutions were analyzed by HPLC (C18-silica column, 0.01 M potassium phosphate buffer pH 4.5 initially, then 0 to 38% acetonitrile over 29 minutes. This gave a retention time of 6.8 min for p-aminobenzoic acid and 26 min for the product. The solutions were kept at room temperature. Analysis by HPLC demonstrated that the N-trichloroacryloyl-p-aminobenzoic acid was stable at least for four days. By this last day the solution of the p-aminobenzoic acid had discolored and additional peaks were seen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650270
Source datasetuspto-grants-1997_07
ORD IDord-3e53379146534db49b785720eb59b4d2
Source noteuspto-grants-1997_07