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5-BROMO-2-METHOXYPHENYLACETONITRILE

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5-BROMO-2-METHOXYPHENYLACETONITRILE Basic information

Product Name:
5-BROMO-2-METHOXYPHENYLACETONITRILE
Synonyms:
  • 5-BROMO-2-METHOXYPHENYLACETONITRILE
  • 2-(5-broMo-2-Methoxyphenyl)acetonitrile
  • Benzeneacetonitrile, 5-broMo-2-Methoxy-
  • 5-BroMo-2-Methoxybenzyl cyanide
  • 5-Bromo-2-methoxybenzyl cyanide, 4-Bromo-2-(cyanomethyl)anisole
  • 5-Bromo-2-methoxybenzeneacetonitrile
CAS:
7062-40-0
MF:
C9H8BrNO
MW:
226.07
Product Categories:
  • Aromatic Nitriles
Mol File:
7062-40-0.mol
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5-BROMO-2-METHOXYPHENYLACETONITRILE Chemical Properties

Melting point:
61-63°C
Boiling point:
182.5-183 °C
Density 
1.450±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37/39
RIDADR 
3439
Hazard Note 
Irritant
HazardClass 
IRRITANT, IRRITANT-HARMFUL
HS Code 
2926907090
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5-BROMO-2-METHOXYPHENYLACETONITRILE Usage And Synthesis

Uses

2-(5-Bromo-2-methoxyphenyl)acetonitrile is a useful intermediate used in the synthesis of 5-bromo-2-methoxyphenylacetonitrile and some of its derivatives.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 38, p. 2050, 1995 DOI: 10.1021/jm00012a004

Synthesis

7035-03-2

7062-40-0

GENERAL METHODS: N-bromosuccinimide (NBS, 1.5 eq., 0.3 mmol), catalyst (10 mol%, 0.02 mmol) and acetonitrile (CH3CN, 1.0 mL) were sequentially added to the reaction tube, followed by o-methoxybenzeneacetonitrile (0.2 mmol). The reaction mixture was stirred at room temperature in a dark environment for 12 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated sodium thiosulfate (Na2S2O3) aqueous solution (2 mL). The reaction mixture was extracted with ethyl acetate (3.5 mL), and the combined organic phases were washed with saturated brine (10 mL), dried over anhydrous sodium sulfate (Na2SO4), and filtered through a diatomaceous earth pad. The filtrate was concentrated under reduced pressure and the residue was purified by fast chromatography on silica gel column with the eluent of petroleum ether/dichloromethane (5:1, v/v) to afford the target product 5-bromo-2-methoxyphenylacetonitrile.

References

[1] Tetrahedron, 2017, vol. 73, # 50, p. 7105 - 7114

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