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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435166Generated: October 28, 2026

Methanol → 1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindoline

https://huagongshe.com/reaction/435166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-Aminophenylacetic acidHCID 14533—
Reactant3-Hydroxyisobenzofuran-1(3H)-oneHCID 3804259—
ReactantCID 24201897HCID 24201897—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-Oxo-2-{p-(carboxymethyl)-phenyl}-isoindolineHCID 1285421994.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400520
Source datasetuspto-grants-1983_08
ORD IDord-e9eccb2a445b4061b843d09713a279f2
Source noteuspto-grants-1983_08