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ChemicalBook--->CAS DataBase List--->150969-56-5

150969-56-5

150969-56-5 Structure

150969-56-5 Structure
IdentificationBack Directory
[Name]

5-(Trifluoromethyl)-1-indanone
[CAS]

150969-56-5
[Synonyms]

5-(TRIFLUOROMETHYL)INDANONE
5-trifluormethyl-1-indanone
5-(Trifluoromethyl)-1-indanone
5-(Trifluoromethyl)indan-1-one 98%
5-(TRIFLUOROMETHYL)-2,3-DIHYDROINDEN-1-ONE,98%
5-(TrifluoroMethyl)-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one, 2,3-dihydro-5-(trifluoromethyl)-
2,3-Dihydro-5-(trifluoromethyl)-1H-inden-1-one, 2,3-Dihydro-1-oxo-5-(trifluoromethyl)-1H-indene
[Molecular Formula]

C10H7F3O
[MDL Number]

MFCD07772122
[MOL File]

150969-56-5.mol
[Molecular Weight]

200.16
Chemical PropertiesBack Directory
[Boiling point ]

237.1±40.0 °C(Predicted)
[density ]

1.347±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2914390090
Spectrum DetailBack Directory
[Spectrum Detail]

5-(Trifluoromethyl)-1-indanone(150969-56-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-bromo-5-(trifluoromethyl)-benzenepropanoic acid

869725-56-4

5-(Trifluoromethyl)-1-indanone

150969-56-5

Step E General procedure for the synthesis of 5-(trifluoromethyl)indan-1-one from 3-[2-bromo-5-(trifluoromethyl)phenyl]propionic acid: to a mixture of 3-[2-bromo-5-(trifluoromethyl)phenyl]propionic acid (2.8 g, 9.4 mmol) in THF (100 mL) and hexanes (20 mL) was added slowly and dropwise at -78°C a solution of 2.5 M n-butyllithium in hexane (8.3 mL). After dropwise addition, the reaction was quenched with saturated aqueous NH4Cl solution. The reaction mixture was extracted twice with ethyl acetate. The combined organic phases were washed with saturated aqueous NaHCO3 and brine, dried over anhydrous MgSO4 and concentrated. The crude product was purified by fast column chromatography on silica gel with 10-20% EtOAc/hexane as eluent to afford the target product 5-(trifluoromethyl)indan-1-one as a white solid (0.7 g, 37% yield).LC/MS analysis: the calculated value of (M+H)+ for C10H7F3O was 201; measured value, 201.1.

[References]

[1] Patent: US2005/261310, 2005, A1. Location in patent: Page/Page column 25
[2] ACS Medicinal Chemistry Letters, 2010, vol. 1, # 9, p. 483 - 487
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