ChemicalBook--->CAS DataBase List--->6342-63-8

6342-63-8

6342-63-8 Structure

6342-63-8 Structure
IdentificationBack Directory
[Name]

1-(2-bromo-5-methoxy-phenyl)ethanone
[CAS]

6342-63-8
[Synonyms]

3-Acetyl-4-bromoanisole
1-(2-bromo-5-methoxy-phenyl)ethanone
ETHANONE 1-(2-BROMO-5-METHOXYPHENYL)-
1-(2-Bromo-5-methoxyphenyl)ethan-1-one, 3-Acetyl-4-bromoanisole
[Molecular Formula]

C9H9BrO2
[MDL Number]

MFCD02683853
[MOL File]

6342-63-8.mol
[Molecular Weight]

229.07
Chemical PropertiesBack Directory
[Melting point ]

102°C
[Boiling point ]

102 °C(Press: 0.4 Torr)
[density ]

1.421±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[color ]

Yellow
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 ]

2914790090
Hazard InformationBack Directory
[Preparation]

Obtained by action of pyridinium chlorochromate with 1-(2-bromo-5-methoxy) ethanol.
[Synthesis]

Benzenemethanol, 2-bromo-5-methoxy-α-methyl-

71095-23-3

1-(2-bromo-5-methoxy-phenyl)ethanone

6342-63-8

General procedure for the synthesis of 1-(2-bromo-5-methoxyphenyl)ethan-1-ol from 1-(2-bromo-5-methoxyphenyl)ethanone: To a solution of 1-(2-bromo-5-methoxyphenyl)ethan-1-ol (3.8 g, 16.5 mmol) in methylene chloride (100 mL) was added pyridinium chlorochromate (PCC, 8.4 g, 33.0 mmol). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the mixture was filtered and the filtrate was concentrated. The crude product was purified by silica gel fast column chromatography with the eluent of petroleum ether/ethyl acetate (5:1) to afford 1-(2-bromo-5-methoxyphenyl)ethanone (3.6 g, 95% yield) as an off-white solid.1H NMR (300 MHz, CDCl3) δ 7.45 (d, 1H), 6.96 (d, 1H), 6.82 (dd, 1H) 4.38 (q, 2H), 3.80 (s, 3H), 2.62 (s, 3H).

[References]

[1] Organic Letters, 2012, vol. 14, # 2, p. 628 - 631
[2] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 7, p. 550 - 554
[3] Patent: WO2013/22740, 2013, A2. Location in patent: Paragraph 0393; 0395
[4] Journal of Organic Chemistry, 2014, vol. 79, # 5, p. 2059 - 2074
[5] Synthetic Communications, 2014, vol. 44, # 14, p. 2076 - 2087
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