HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 4-Aminobenzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | N-Trichloroacryloyl-p-aminobenzoic acid | HCID 19032249 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Aminobenzoic Acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650270 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-3e53379146534db49b785720eb59b4d2 |
| Source note | uspto-grants-1997_07 |