ChemicalBook--->CAS DataBase List--->19967-55-6

19967-55-6

19967-55-6 Structure

19967-55-6 Structure
IdentificationBack Directory
[Name]

1-Bromo-3-methyl-2-butanone
[CAS]

19967-55-6
[Synonyms]

1-BROMO-3-METHYL-2-BUTANONE
1-Bromo-3-methylbutan-2-one
2-BroMo-1-isopropylethanone
Bromomethyl isopropyl ketone
Isopropyl bromomethyl ketone
2-Butanone, 1-bromo-3-methyl-
1-BroMo-3,3-diMethyl-2-propanone
1-BroMo-3-Methylbutan-2-one, 95+%
[Molecular Formula]

C5H9BrO
[MDL Number]

MFCD00015716
[MOL File]

19967-55-6.mol
[Molecular Weight]

165.03
Chemical PropertiesBack Directory
[Boiling point ]

164 °C
[density ]

1.355
[refractive index ]

1.4685
[Fp ]

56 °C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[solubility ]

Chloroform, Ethyl Acetate
[form ]

Oil
[color ]

Clear Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2914120000
Spectrum DetailBack Directory
[Spectrum Detail]

1-Bromo-3-methyl-2-butanone(19967-55-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Methyl-2-butanone

563-80-4

1-Bromo-3-methyl-2-butanone

19967-55-6

Example 1 Synthesis of 1-bromo-3-methylbutan-2-one: (1) Bromine (12.9 mL, 250 mmol) was added slowly and dropwise to an ethanol (EtOH, 250 mL) solution of 3-methyl-2-butanone (25.8 g, 300 mmol) under ice bath cooling conditions. The reaction mixture was stirred continuously for 2 h in an ice bath. After completion of the reaction, it was diluted by adding petroleum ether (600 mL). The organic phase was separated and washed twice with distilled water. The combined aqueous phases were back-extracted twice with petroleum ether. All organic phases were combined and washed twice each with cold sodium carbonate solution and saturated saline in that order. The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure at room temperature to afford the target product 1-bromo-3-methylbutan-2-one in 50% yield.

[References]

[1] Patent: US5910506, 1999, A
[2] Patent: WO2007/14921, 2007, A1. Location in patent: Page/Page column 69
[3] Patent: WO2003/106455, 2003, A1. Location in patent: Page 60
[4] Patent: WO2007/14922, 2007, A1. Location in patent: Page/Page column 79-80
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 8, p. 2922 - 2926
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