ChemicalBook--->CAS DataBase List--->67159-85-7

67159-85-7

67159-85-7 Structure

67159-85-7 Structure
IdentificationBack Directory
[Name]

5-bromo-2,3-dihydro-3,3-dimethylinden-1-one
[CAS]

67159-85-7
[Synonyms]

5-bromo-3,3-dimethyl-1-indanone
5-bromo-2,3-dihydro-3,3-dimethylinden-1-one
5-Bromo-3,3-dimethyl-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one, 5-bromo-2,3-dihydro-3,3-dimethyl-
[Molecular Formula]

C11H11BrO
[MDL Number]

MFCD27927273
[MOL File]

67159-85-7.mol
[Molecular Weight]

239.11
Chemical PropertiesBack Directory
[Melting point ]

123-125 °C(Solv: ethanol (64-17-5))
[Boiling point ]

314.5±41.0 °C(Predicted)
[density ]

1.409±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Chemical Properties]

Colorless liquid
[Synthesis]

6-bromo-1,1-dimethylindan

67159-88-0

5-bromo-2,3-dihydro-3,3-dimethylinden-1-one

67159-85-7

6-Bromo-1,1-dimethyl-2,3-dihydro-1H-indene (3.6 g, 16 mmol) was used as a raw material and dissolved in acetic acid (50 mL). Subsequently, an oxidizer solution prepared from CrO3 (9.6 g, 96.0 mmol) dissolved in 50% aqueous acetic acid (50 mL) was added to this solution. The reaction mixture was heated and stirred at 60 °C for 3 hours. Upon completion of the reaction, the reaction was quenched by addition of isopropanol (20 mL). The quenched reaction mixture was partitioned between EtOAc (200 mL) and 0.25 M NaOH aqueous solution (100 mL). The organic layer was separated and the aqueous phase was further extracted with EtOAc (2 × 100 mL). All organic phases were combined, washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. Purification by rapid chromatography on silica gel (with 50% EtOAc/hexane as eluent) afforded the target product 5-bromo-3,3-dimethyl-2,3-dihydro-1H-inden-1-one (2.91 g, 76% yield) as a white solid. The product was confirmed by 1H NMR (400 MHz, chloroform-d): δ 7.65 (s, 1H), 7.47-7.58 (m, 2H), 2.58 (s, 2H), 1.42 (s, 6H); mass spectrum (EI) m/z = 240.1 [M + 1]+.

[References]

[1] Patent: EP2236500, 2010, A1. Location in patent: Page/Page column 39-40
[2] Patent: US2012/225857, 2012, A1. Location in patent: Page/Page column 24
[3] Patent: US2006/173183, 2006, A1. Location in patent: Page/Page column 123
Spectrum DetailBack Directory
[Spectrum Detail]

5-bromo-2,3-dihydro-3,3-dimethylinden-1-one(67159-85-7)1HNMR
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