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3-(BENZYLOXY)-5-BROMOPYRIDINE

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3-(BENZYLOXY)-5-BROMOPYRIDINE Basic information

Product Name:
3-(BENZYLOXY)-5-BROMOPYRIDINE
Synonyms:
  • 3-(BENZYLOXY)-5-BROMOPYRIDINE
  • 3-(Benzyloxy)-5-bromopyridine ,97%
  • B67304
  • 5-Benzyloxy-3-broMopyridine
  • 3-Bromo-5-bezyloxypyridine
  • C12H10BrNO 3-(BENZYLOXY)-5-BROMOPYRIDINE
  • 3-bromo-5-phenylmethoxypyridine
  • 3-Benzyloxy-5-bromopyridine >
CAS:
130722-95-1
MF:
C12H10BrNO
MW:
264.12
Product Categories:
  • pharmacetical
Mol File:
130722-95-1.mol
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3-(BENZYLOXY)-5-BROMOPYRIDINE Chemical Properties

Melting point:
69.0 to 73.0 °C
Boiling point:
343.7±27.0 °C(Predicted)
Density 
1.438±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
2.23±0.10(Predicted)
color 
White to Light yellow
λmax
290nm(MeOH)(lit.)
InChI
InChI=1S/C12H10BrNO/c13-11-6-12(8-14-7-11)15-9-10-4-2-1-3-5-10/h1-8H,9H2
InChIKey
YSHKYZAWTWKQKK-UHFFFAOYSA-N
SMILES
C1=NC=C(OCC2=CC=CC=C2)C=C1Br
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
29333990
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3-(BENZYLOXY)-5-BROMOPYRIDINE Usage And Synthesis

Chemical Properties

White solid

Synthesis

625-92-3

100-51-6

130722-95-1

1. benzyl alcohol (4.60 g, 42.6 mmol) was slowly added dropwise to a stirred suspension of sodium hydride (60% mineral oil dispersion, 1.70 g, 42.5 mmol) in dimethylformamide (DMF, 50 mL) under dry conditions. 2. the reaction mixture was heated to 60 °C and stirred at this temperature for 1 h to ensure complete deprotonation. 3. 3,5-dibromopyridine (10.0 g, 42.2 mmol) was dissolved in dimethylformamide (DMF, 20 mL) and this solution was subsequently added to the above reaction mixture. 4. The reaction system was warmed to 80 °C and the reaction was continued with stirring for 2 hours to complete the nucleophilic substitution reaction. 5. Upon completion of the reaction, the reaction mixture was cooled to room temperature and subsequently separated by extraction with ethyl acetate and water. 6. The organic layer was separated and dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. 7. The crude product was purified by fast column chromatography to afford the target compound 3-benzyloxy-5-bromopyridine (4.75 g, 43% yield). 8. Mass spectrometry (MS) analysis showed the following: m/z calculated value (M + H) + 265, measured value 265, as expected.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 12, p. 3150 - 3155
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 2, p. 717 - 724
[3] Patent: US2013/184313, 2013, A1. Location in patent: Paragraph 1099; 1100
[4] Tetrahedron, 2011, vol. 67, # 26, p. 4767 - 4773
[5] Tetrahedron, 2001, vol. 57, # 20, p. 4447 - 4454

3-(BENZYLOXY)-5-BROMOPYRIDINE Preparation Products And Raw materials

Raw materials

3-(BENZYLOXY)-5-BROMOPYRIDINESupplier

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