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6-Chloro-1-indanone

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6-Chloro-1-indanone Basic information

Product Name:
6-Chloro-1-indanone
Synonyms:
  • JR-6918, 6-Chloro-2,3-dihydroinden-1-one, 97%
  • 6-CHLORO-1-INDANONE 96
  • 6-Chloro-1-indanone
  • 6-choroindanone
  • 6-Chloro-2,3-dihydro-1H-inden-1-one
  • 1H-Inden-1-one, 6-chloro-2,3-dihydro-
  • 6-Chloro-1-indanone, 97+%
CAS:
14548-38-0
MF:
C9H7ClO
MW:
166.6
EINECS:
627-183-5
Product Categories:
  • Building Blocks
  • C9
  • Carbonyl Compounds
  • Chemical Synthesis
  • Ketones
  • Organic Building Blocks
  • API intermediates
Mol File:
14548-38-0.mol
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6-Chloro-1-indanone Chemical Properties

Melting point:
71-79 °C
Boiling point:
110 °C(Press: 0.01 Torr)
Density 
1.312±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
Appearance
White to off-white Solid
InChIKey
SMSGJDOJSQHQIW-UHFFFAOYSA-N
CAS DataBase Reference
14548-38-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
2
HazardClass 
IRRITANT
HS Code 
2914790090
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6-Chloro-1-indanone Usage And Synthesis

Uses

6-Chloro-1-indanone is a chlorinated indanone compound. It is a crucial compound that could be used as a pharmaceutical intermediate in pharmaceutical synthesis and scientific research.

Synthesis

2019-34-3

14548-38-0

General procedure for the synthesis of 6-chloro-2,3-dihydroinden-1-one from 3-(4-chlorophenyl)propionic acid: trifluoromethanesulfonic acid (3 equiv.) was slowly added to an anhydrous solution of 3-(4-chlorophenyl)propionic acid (0.5 mmol) in anhydrous dichloromethane (1.0 mL) in a 12 mL Q-tube ?pressure tube (supplied by QLabtech) at 0 °C. . The reaction mixture was then warmed to room temperature. A PTFE septum was placed on top of the reaction tube and sealed using the appropriate cap and pressure adapter. The sealed reaction tube was heated in an oil bath at 80°C. The progress of the reaction was monitored by thin layer chromatography (TLC) and gas chromatography-mass spectrometry (GC/MS) until the feedstock completely disappeared. After completion of the reaction, the mixture was poured into ice water and extracted three times with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Finally, the target compound 6-chloro-2,3-dihydroinden-1-one was purified from the crude product by fast column chromatography.

References

[1] Molecules, 2014, vol. 19, # 5, p. 5599 - 5610
[2] Patent: WO2017/150904, 2017, A1. Location in patent: Paragraph 402-404
[3] Synthetic Communications, 2007, vol. 37, # 13, p. 2171 - 2177
[4] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 8, p. 2554 - 2558
[5] Polish Journal of Chemistry, 1991, vol. 65, # 11, p. 2057 - 2060

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