Basic information Safety Supplier Related

4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE

Basic information Safety Supplier Related

4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE Basic information

Product Name:
4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE
Synonyms:
  • 4-chloro-2,3-dihydro-1H-indol-2-one
  • 4-Chloro-2-oxindole 4-Chloro-1,3-dihydro-indol-2-one in stock Factory
  • 4-CHLOROOXINDOLE
  • 4-CHLORO-2-OXINDOLE
  • 4-CHLORO-1,3-DIHYDRO-2H-INDOL-2-ONE
  • 4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE
  • AKOS 207-07
  • 4-Chloro-2-oxoindole
CAS:
20870-77-3
MF:
C8H6ClNO
MW:
167.59
Product Categories:
  • Halides
  • Pyrroles & Indoles
Mol File:
20870-77-3.mol
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4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE Chemical Properties

Melting point:
206-208°
Boiling point:
340.3±42.0 °C(Predicted)
Density 
1.362±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
powder
pka
13.27±0.20(Predicted)
color 
yellow
InChI
InChI=1S/C8H6ClNO/c9-6-2-1-3-7-5(6)4-8(11)10-7/h1-3H,4H2,(H,10,11)
InChIKey
XNSPDJAXCBZCRV-UHFFFAOYSA-N
SMILES
N1C2=C(C(Cl)=CC=C2)CC1=O
CAS DataBase Reference
20870-77-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933790090
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4-CHLORO-1,3-DIHYDRO-INDOL-2-ONE Usage And Synthesis

Synthesis

6344-05-4

20870-77-3

The general procedure for the synthesis of 4-chloro-2-oxoindole (4-chloroindolone) from 4-chloroindoline-2,3-dione was as follows: titanium tetrachloride (TiCl4) (0.7 mL, 6 mmol) was slowly added to a stirring suspension of zinc powder (0.78 g, 12 mmol) in freshly distilled anhydrous THF (15 mL) at room temperature and under dry nitrogen atmosphere. After addition, the mixture was refluxed for 2 hours. After the formed suspension of low-valent titanium reagent was cooled, a THF (10 mL) solution of indigo red or its derivative (2 mmol) was added dropwise. The reaction mixture was stirred at room temperature for about 5 min under nitrogen protection. After confirming the completion of the reaction by thin layer chromatography (TLC) analysis, the reaction was quenched with 3% hydrochloric acid (15 mL) and subsequently extracted with chloroform (3 x 50 mL). The organic phases were combined, washed with water (3 x 50 mL) and dried over anhydrous sodium sulfate. After concentration of the solvent under reduced pressure, the crude product was purified by column chromatography (petroleum ether/ethyl acetate = 5:1) to afford the target compound 4-chloro-2-oxindole (4-chloroindolone).

References

[1] Tetrahedron Letters, 2014, vol. 55, # 14, p. 2238 - 2242

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