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BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE

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BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE Basic information

Product Name:
BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE
Synonyms:
  • BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE
  • BIS(2,2,2-TRIFLUOROETHYL) PHOSPHONATE
  • PHOSPHONIC ACID BIS(2,2,2-TRIFLUOROETHYL) ESTER
  • PHOSPHOROUS ACID BIS(2,2,2-TRIFLUOROETHYL) ESTER
  • BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE, TEC H., 90%
  • Bis(2,2,2-trifluoroethyl) phosphite,Phosphonic acid bis(2,2,2-trifluoroethyl) ester
  • Bis(2,2,2-trifluoroethyl) Phosphonate Phosphonic Acid Bis(2,2,2-trifluoroethyl) Ester Phosphorous Acid Bis(2,2,2-trifluoroethyl) Ester
  • Bis(2,2,2-trifluoroethyl) phosphite technical grade, 90%
CAS:
92466-70-1
MF:
C4H5F6O3P
MW:
246.04
Mol File:
92466-70-1.mol
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BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE Chemical Properties

Boiling point:
43-44 °C/2 mmHg (lit.)
Density 
1.545 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.332(lit.)
Flash point:
169 °F
form 
Liquid
color 
Colorless to Almost colorless
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
23-26-28-36
WGK Germany 
3
HS Code 
2920.90.5100

MSDS

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BIS(2,2,2-TRIFLUOROETHYL) PHOSPHITE Usage And Synthesis

Uses

Bis(2,2,2-trifluoroethyl) phosphite was used in the synthesis of bis(2,2,2-trifluoroethyl phosphorochloridate. It was also employed as reagent for the synthesis of mono- and diesters of phosphorous acid.

Synthesis Reference(s)

Synthesis, p. 410, 1984 DOI: 10.1055/s-1984-30856

Synthesis

The synthesis method of Bis(2,2,2-trifluoroethyl) Phosphite is as follows: A solution of phosphorus trichloride (43.5 mL, 0.50 mol) in dichloromethane (100 mL) was placed in an oven dried 1L round bottom flask. A reflux condenser and pressure equalizing addition funnel were attached to the round bottom flask. The addition funnel was charged with a solution of 2-methyl-2-propanol (48.0 mL, 0.50 mol) in dichloromethane (100 mL), and then the contents of the addition funnel were added in a dropwise manner to the round bottom flask under argon gas at 0 ℃over the course of 30 min. The reaction mixture was allowed to stir for an additional 30 min, then the addition funnel is recharged with a solution of 2,2,2-trifluoroethanol (70.0 mL, 0.96 mol) and dichloromethane (100 mL) and then the contents of the addition funnel were added in a dropwise manner to the round bottom flask under argon gas at 0 ℃ over the course of 30 min. The reaction mixture was then allowed to stir at RT overnight. The gaseous vapors were then degassed into NaOH (30.2 g, 0.98 mol) in 200 mL of water over the course of 8 hrs. The solvents were removed by rotary evaporation and the crude material was fractionally distilled under reduced pressure yielding Bis(2,2,2-trifluoroethyl) Phosphite (100.89 g, 0.41 mol, 82.2%) as colorless liquid.

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