Basic information Safety Supplier Related

2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE

Basic information Safety Supplier Related

2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE Basic information

Product Name:
2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE
Synonyms:
  • 2,3-DIHYDRO-CYCLOPENTA[A]NAPHTHALEN-1-ONE
  • 2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE
  • 2,3-Dihydro-1H-cyclopenta[a]naphthalen-1-one
  • 1H-Benz[e]inden-1-one, 2,3-dihydro-
  • (S)-2-amino-1-(3,5-dimethylphenyl)ethan-1-ol
CAS:
6342-87-6
MF:
C13H10O
MW:
182.22
Mol File:
6342-87-6.mol
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2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE Chemical Properties

Melting point:
103 °C
Boiling point:
348.6±12.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
2-8°C
Appearance
White to off-white Solid
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2,3-DIHYDRO-1H-BENZ[E]INDEN-1-ONE Usage And Synthesis

Synthesis

21658-35-5

6342-87-6

In a flask equipped with a mechanical stirrer, Eaton's reagent prepared by adding 144.0 g of P4O10 and 840 mL of methanesulfonic acid was added in batches at room temperature. Subsequently, 144.0 g (~720 mmol) of 3-(2-naphthyl)propionic acid was added to the system. The reaction mixture was stirred overnight and then slowly poured into 2 L of ice-cold water to quench the reaction. The crude product was extracted with 3 x 500 mL dichloromethane and the organic phases were combined. The organic phase was washed sequentially with aqueous K2CO3, dried over anhydrous Na2SO4 and concentrated to dryness under reduced pressure. The residue was purified by fast column chromatography using 600 mL silica gel 60 (40-63 μm) as stationary phase and hexane and dichloromethane (1:1, v/v) as eluent to afford 105.0 g (80% yield) of the target compound, 2,3-dihydro-1H-benzo[e]inden-1-one, as a brown solid. Elemental analysis (C13H10O) Calculated values: C, 85.69; H, 5.53. Measured values: C, 85.98; H, 5.75. 1H NMR (CDCl3) δ: 9.12 (d, J = 8.5 Hz, 1H), 7.93 (d, J = 8.3 Hz, 1H), 7.81 (d, J = 8.1 Hz, 1H), 7.61 (ddd , J = 8.3, 7.1, 1.2 Hz, 1H), 7.50 (ddd, J = 8.1, 7.1, 1.0 Hz, 1H), 7.39 (d, J = 8.3 Hz, 1H), 3.12-3.04 (m, 2H), 2.75-2.65 (m, 2H). 13C{1H} NMR (CDCl3) δ: 207.26, 158.26, 135.47 158.26, 135.47, 132.41, 130.81, 129.23, 128.65, 127.90, 126.39, 123.87, 123.76, 36.73, 25.99.

References

[1] Journal of the American Chemical Society, 2001, vol. 123, # 14, p. 3214 - 3222
[2] Chemistry - A European Journal, 2015, vol. 21, # 37, p. 13052 - 13057
[3] Patent: WO2017/118617, 2017, A1. Location in patent: Page/Page column 20
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 1845 - 1848
[5] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1983, vol. 22, # 10, p. 1015 - 1019

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