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di(naphthalen-2-yl)phosphine oxide

Product Name
di(naphthalen-2-yl)phosphine oxide
CAS No.
78871-05-3
Chemical Name
di(naphthalen-2-yl)phosphine oxide
Synonyms
Di(2-naphthyl)phosphine Oxide;2,3-dinaphthyl phosphine oxide;Bis(2-naphthyl)phosphine oxide;dinaphthalen-2-yl(oxo)phosphanium;di-2-naphthalenyl-Phosphine oxide;di(naphthalen-2-yl)phosphine oxide;Phosphine oxide, di-2-naphthalenyl-;bis[naphthalen-2-yl]phosphine oxide
CBNumber
CB72715378
Molecular Formula
C20H15OP
Formula Weight
302.31
MOL File
78871-05-3.mol
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di(naphthalen-2-yl)phosphine oxide Property

Melting point:
90.4-92.0 °C
Boiling point:
513.9±33.0 °C(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Off-white to light yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Ambeed
Product number
A109288
Product name
Di(naphthalen-2-yl)phosphineoxide
Purity
97%
Packaging
250mg
Price
$21
Updated
2021/12/16
Arctom
Product number
AS433728
Product name
Di(naphthalen-2-yl)phosphineoxide
Purity
97%
Packaging
250mg
Price
$21
Updated
2021/12/16
Arctom
Product number
AS433728
Product name
Di(naphthalen-2-yl)phosphineoxide
Purity
97%
Packaging
1g
Price
$47
Updated
2021/12/16
Ambeed
Product number
A109288
Product name
Di(naphthalen-2-yl)phosphineoxide
Purity
97%
Packaging
1g
Price
$47
Updated
2021/12/16
Chemenu
Product number
CM262996
Product name
Di(naphthalen-2-yl)phosphineoxide
Purity
95%
Packaging
5g
Price
$122
Updated
2021/12/16
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di(naphthalen-2-yl)phosphine oxide Chemical Properties,Usage,Production

Synthesis

762-04-9

78871-05-3

A mixed solution of magnesium (2.94 g, 1.0 eq.), a small amount of iodine and a small amount of 1,2-dibromoethane in THF (30 mL) was stirred at room temperature for 1 hour under argon protection. Warmed to 35 °C, a solution of 2-bromonaphthalene (25 g, 0.121 mol) in THF (20 mL) was slowly added, followed by stirring the reaction mixture at 40 °C for 30 min. Cooled to 5 °C, a solution of diethyl phosphite (9.77 g, 0.5 eq.) in THF (10 mL) was added dropwise and stirring was continued for 3 h at 5 °C maintaining the temperature. Upon completion of the reaction, water (20 mL) was added at 3 °C, followed by toluene (60 mL) and 6 M hydrochloric acid (20 mL) and stirred at room temperature for 30 min. The organic phase was separated and washed sequentially with water (10 mL), 5% aqueous sodium bicarbonate (10 mL) and 5% aqueous sodium chloride (10 mL). The organic layer was dried over anhydrous magnesium sulfate, gravity filtered and the filtrate was concentrated under reduced pressure. The resulting residue was recrystallized with diisopropyl ether-heptane mixed solvent to afford white crystals of 2,2'-bis-(2-naphthalenyl)phosphine oxide (9.62 g, 53.0% yield) with a melting point of 98.3 °C. The product was purified by NMR hydrogen spectroscopy. The structure of the product was confirmed by nuclear magnetic resonance hydrogen (1H-NMR, 300 MHz, CDCl3, TMS), carbon (13C-NMR, 75 MHz, CDCl3) and phosphorus (31P-NMR, 121 MHz, CDCl3, 85% H3PO4) spectra.

References

[1] Patent: EP1452537, 2004, A1. Location in patent: Page 30

di(naphthalen-2-yl)phosphine oxide Preparation Products And Raw materials

Raw materials

Preparation Products

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78871-05-3, di(naphthalen-2-yl)phosphine oxideRelated Search:


  • di(naphthalen-2-yl)phosphine oxide
  • di-2-naphthalenyl-Phosphine oxide
  • dinaphthalen-2-yl(oxo)phosphanium
  • bis[naphthalen-2-yl]phosphine oxide
  • Phosphine oxide, di-2-naphthalenyl-
  • Bis(2-naphthyl)phosphine oxide
  • 2,3-dinaphthyl phosphine oxide
  • Di(2-naphthyl)phosphine Oxide
  • 78871-05-3