2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Basic information
- Product Name:
- 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
- Synonyms:
-
- 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
- 5-Bromo-1,3-dihydro-2H-inden-2-one
- 5-Bromoindan-2-one
- 2-Indanone, 5-broMo-
- 5-bromo-1,3-dihydroinden-2-one
- 5-BROMO-1H-INDEN-2(3H)-ONE
- 5-Bromo-2-indanone
- 5-broMo-2,3-dihydro-1H-inden-2-one
- CAS:
- 174349-93-0
- MF:
- C9H7BrO
- MW:
- 211.06
- Mol File:
- 174349-93-0.mol
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Chemical Properties
- Boiling point:
- 299.5±40.0 °C(Predicted)
- Density
- 1.608±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to yellow Solid
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Usage And Synthesis
Synthesis
75476-78-7
174349-93-0
The general procedure for the synthesis of 5-bromo-2-indanone from 5-bromo-1H-indene was as follows: first, 1.5 L of 30% H2O2 and 300 mL of formic acid were added to a reaction flask, and the temperature of the reaction was controlled at 35 °C. Subsequently, 148 g of 5-bromo-1H-indene was added to the reaction mixture at 40 °C. The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, a large amount of water was added to the reaction mass to precipitate a white solid, which was subsequently filtered. Next, 3 L of 5% aqueous sulfuric acid solution was added to the flask and heated to boiling. The white solid reactant was added to the flask and connected to a distillation unit to obtain a final 64 g of 5-bromo-2-indanone (white solid).
References
[1] Patent: JP2016/29040, 2016, A. Location in patent: Paragraph 0060
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