HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Aminophenylacetic acid | HCID 14533 | — |
| Reactant | 3-Hydroxyisobenzofuran-1(3H)-one | HCID 3804259 | — |
| Reactant | CID 24201897 | HCID 24201897 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline | HCID 12854219 | 94.3% |
Reaction Steps
1.5 g of o-phthalaldehydic acid and 1.5 g of p-aminophenylacetic acid were added to 30 ml of methanol to form a mixture which was agitated at room temperature for one hour and incorporated with 0.54 g of potassium boron hydride in several portions. Then, the whole was reacted at room temperature of 5 hours and then freed from the solvent under a reduced pressure. The resulting residue was incorporated with 50 ml of water and then with a small amount of acetic acid to obtain an acidic solution, after which crystals precipitated from the thus obtained solution were filtered off, dried and recrystallized from ethanol to obtain 2.5 g of 1-oxo-2 -{p-(carboxymethyl)-phenyl}-isoindoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04400520 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-e9eccb2a445b4061b843d09713a279f2 |
| Source note | uspto-grants-1983_08 |