Basic information Safety Supplier Related

2-Oxo-indoline-4-carboxylic acid

Basic information Safety Supplier Related

2-Oxo-indoline-4-carboxylic acid Basic information

Product Name:
2-Oxo-indoline-4-carboxylic acid
Synonyms:
  • 2-Oxo-indoline-4-carboxylic acid
  • 4-Carboxyoxindole
  • 2,3-Dihydro-2-oxo-1H-indole-4-carboxylic acid
  • 4-Carboxyl-2-oxindole
  • 2-oxo-2,3-dihydro-1H-indole-4-carboxylic acid
  • 1H-Indole-4-carboxylic acid, 2,3-dihydro-2-oxo-
CAS:
90322-37-5
MF:
C9H7NO3
MW:
177.16
Mol File:
90322-37-5.mol
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2-Oxo-indoline-4-carboxylic acid Chemical Properties

Boiling point:
444.2±45.0 °C(Predicted)
Density 
1.433
storage temp. 
Sealed in dry,Room Temperature
pka
3.63±0.20(Predicted)
Appearance
Yellow to brown Solid
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Safety Information

HS Code 
2933998090
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2-Oxo-indoline-4-carboxylic acid Usage And Synthesis

Synthesis

90924-46-2

90322-37-5

The general procedure for the synthesis of 2-indolone-4-carboxylic acid from 4-carboxylic acid methyl ester dihydroindol-2-one was as follows: to a 50 mL round-bottomed flask was added 2-oxo-2,3-dihydro-1H-indole-4-carboxylic acid methyl ester (150 mg, 0.78 mmol, 1.00 equiv.), methanol (2 mL) and tetrahydrofuran (8 mL). An aqueous solution (5 mL) of LiOH (150.8 mg, 6.30 mmol, 8.00 equiv) was subsequently added. The reaction mixture was stirred at 25 °C overnight. After completion of the reaction, the solvent was concentrated under reduced pressure. The residue was diluted with distilled water (20 mL) and washed with ethyl acetate (30 mL). The pH of the aqueous phase was adjusted to 6 with 1 mol/L HCl. The aqueous phase was extracted with ethyl acetate (2 x 40 mL), the organic phases were combined and dried over anhydrous sodium sulfate. The dried organic phase was concentrated under reduced pressure to afford 2-oxo-2,3-dihydro-1H-indole-4-carboxylic acid (85 mg, 61% yield) as a light brown solid. Mass spectrum (electrospray, m/z) [M + H]+: 178.

References

[1] Patent: WO2017/205296, 2017, A1. Location in patent: Paragraph 225

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