di(naphthalen-1-yl)phosphine oxide
di(naphthalen-1-yl)phosphine oxide Basic information
- Product Name:
- di(naphthalen-1-yl)phosphine oxide
- Synonyms:
-
- di(naphthalen-1-yl)phosphine oxide
- di-1-naphthalenyl-Phosphine oxide
- Phosphine oxide, di-1-naphthalenyl-
- Bis(1-naphthyl)phosphine oxide
- CAS:
- 13440-07-8
- MF:
- C20H15OP
- MW:
- 302.31
- Mol File:
- 13440-07-8.mol
di(naphthalen-1-yl)phosphine oxide Chemical Properties
- Melting point:
- 164.9-165.6 °C
- Boiling point:
- 513.9±33.0 °C(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- Appearance
- White to off-white Solid
di(naphthalen-1-yl)phosphine oxide Usage And Synthesis
Synthesis
762-04-9
13440-07-8
A tetrahydrofuran solution (60 mL) of magnesium scrapings (2.94 g, 2.00 eq.), a small amount of iodine and 1,2-dibromoethane was stirred at room temperature for 1 hour under argon protection. Subsequently, a tetrahydrofuran solution (20 mL) of 2-bromonaphthalene (25.00 g, 2.00 eq.) was slowly added dropwise at 27°C and the reaction mixture was warmed up to 40°C with continued stirring for 45 minutes. Next, the reaction system was cooled to -9°C, a tetrahydrofuran solution (10 mL) of diethyl phosphite (9.77 g, 0.06 mol) was added dropwise and the reaction was stirred at 2°C for 3 hours. Upon completion of the reaction, the temperature of the system was adjusted to -5°C and the reaction was quenched by the slow addition of water (20 mL), followed by the addition of toluene (60 mL) and 6 M hydrochloric acid (20 mL) for extraction. The organic layer was separated and washed sequentially with 5% aqueous sodium bicarbonate and 5% aqueous sodium chloride. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting crude product was recrystallized with isopropyl ether/hexane mixed solvent and dried (under reduced pressure, 40°C) to give 1,1'-dinaphthylphosphine oxide (9.621 g, white powder) in 53.0% yield. The structure of the product was confirmed by 1H-NMR (300 MHz, CDCl3, TMS), 13C-NMR (75 MHz, CDCl3) and 31P-NMR (121 MHz, CDCl3, 85% H3PO4).
References
[1] Patent: EP1626052, 2006, A1. Location in patent: Page/Page column 7
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