HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435167Generated: October 29, 2026
Methanol → 1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline
https://huagongshe.com/reaction/435167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Aminophenylacetic acid | HCID 14533 | — |
| Reactant | CID 24201897 | HCID 24201897 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline | HCID 12854219 | — |
Reaction Steps
1.64 g of o-phthalaldehydic acid methyl ester 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. The whole was reacted at room temperature for 15 hours and freed from the solvent by distillation at a reduced pressure to obtain a residue. The thus obtained residue was incorporated with 50 ml of water and then with a small amount of acetic acid to form an acidic solution, after which crystals precipitated from said solution were filtered off, dried and recrystallized from ethanol thereby to obtain 2.4 g of 1-oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline having the following properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400520 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-74063f74ac52448b9d4230492e073fbe |
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| Source note | uspto-grants-1983_08 |
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