Basic information Safety Supplier Related

DIETHYL 4-BROMOBENZYL PHOSPHONATE

Basic information Safety Supplier Related

DIETHYL 4-BROMOBENZYL PHOSPHONATE Basic information

Product Name:
DIETHYL 4-BROMOBENZYL PHOSPHONATE
Synonyms:
  • DIETHYL 4-BROMOBENZYL PHOSPHONATE
  • 4-BROMOBENZYL-PHOSPHONIC ACID DIETHYLESTER
  • Diethy 4-Bromobenzyl Phosphonate
  • Diethyl(4-Bromobenzyl)phosphonate>
  • Phosphonic acid, P-[(4-bromophenyl)methyl]-, diethyl ester
  • 4-Bromobenzyl diethylphosphite
  • Diethyl P-[(4-bromophenyl)methyl]phosphonate
CAS:
38186-51-5
MF:
C11H16BrO3P
MW:
307.12
Product Categories:
  • Piperidines ,Homopiperidines
  • Horner-Emmons Reaction
  • Synthetic Organic Chemistry
  • Wittig & Horner-Emmons Reaction
Mol File:
38186-51-5.mol
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DIETHYL 4-BROMOBENZYL PHOSPHONATE Chemical Properties

Boiling point:
183 °C / 0.6mmHg
Density 
1.37
refractive index 
1.5230-1.5270
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Almost colorless
CAS DataBase Reference
38186-51-5
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Safety Information

HS Code 
2931.90.6000
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DIETHYL 4-BROMOBENZYL PHOSPHONATE Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

Diethyl 4-Bromobenzylphosphonate can be used as a virucide.

Synthesis

589-15-1

122-52-1

38186-51-5

General procedure for the synthesis of diethyl 4-bromobenzylphosphonate (16) from p-bromobenzyl bromide and triethyl phosphite: 1-bromo-4-(bromomethyl)benzene (5.0 g, 20 mmol) and triethyl phosphite (51 mL, 300 mmol) were added to a round-bottomed flask, and the mixture was reacted by refluxing the reaction for 19 hours at 90 °C. Upon completion of the reaction, the excess triethyl phosphite was removed by distillation under reduced pressure. The crude product was purified by fast column chromatography (eluent ratio 1:1 hexane/ethyl acetate) to afford the target compound 16 in 98% yield. The product was a colorless liquid; 1H NMR (400 MHz, CDCl3) δ 7.30 (d, 2H, J = 7.5 Hz), 7.05 (d, 2H, J = 7.6 Hz), 3.99-3.88 (m, 4H), 2.99 (s, 1H), 2.94 (s, 1H), 1.12 (t, 6H, J = 6.9 Hz); 13C NMR ( 100 MHz, CDCl3) δ 131.7, 131.6, 131.5, 121.0, 62.3, 34.0, 32.0, 16.5; HRMS calculated value (C11H16BrO3P, [M + H]+) 307.0097, measured value 307.0093.

References

[1] Patent: US6689922, 2004, B1. Location in patent: Page column 23
[2] Chemistry - A European Journal, 2012, vol. 18, # 24, p. 7473 - 7485
[3] Synthetic Communications, 2011, vol. 41, # 2, p. 206 - 218
[4] Patent: US2013/41153, 2013, A1. Location in patent: Paragraph 0041; 0042; 0043; 0044
[5] ChemMedChem, 2010, vol. 5, # 1, p. 56 - 60

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