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1067-71-6

1067-71-6 Structure

1067-71-6 Structure
IdentificationMore
[Name]

Diethyl (2-oxopropyl)phosphonate
[CAS]

1067-71-6
[Synonyms]

ACETYLPHOSPHONIC ACID DIETHYL ESTER
AURORA KA-1476
DIETHYL(2-OXOPROPYL)PHOSPHONATE
DIETHYL ACETYLPHOSPHONATE
(2-Oxo-propyl)-phosphonicaciddiethylester
Diethyl(2-oxopropyl)phosphonate, 97 %
Diethyl acetylmethylphosphonate, 97%
Diethyl 2-oxopropylphosphonate Diethyl Acetyl Methyl Phosphonate
[EINECS(EC#)]

682-094-9
[Molecular Formula]

C7H15O4P
[MDL Number]

MFCD00044728
[Molecular Weight]

194.17
[MOL File]

1067-71-6.mol
Chemical PropertiesBack Directory
[Appearance]

CLEAR COLORLESS TO LIGHT YELLOW LIQUID
[Boiling point ]

126 °C9 mm Hg(lit.)
[density ]

1.01 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.433(lit.)
[Fp ]

>230 °F
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Miscible with tetrahydrofuran, ether, dichloromethane and chloroform.
[form ]

Liquid
[color ]

Clear colorless to light yellow
[InChI]

InChI=1S/C7H15O4P/c1-4-10-12(9,11-5-2)6-7(3)8/h4-6H2,1-3H3
[InChIKey]

RSAFKRSMGOSHRK-UHFFFAOYSA-N
[SMILES]

P(CC(=O)C)(=O)(OCC)OCC
[CAS DataBase Reference]

1067-71-6(CAS DataBase Reference)
Questions And AnswerBack Directory
[Preparation]

The synthesis steps of Diethyl (2-oxopropyl)phosphonate are as follows: S1. Add 5 kg of triethyl phosphite and 2 kg of chloroacetone to a reaction vessel, reflux at 120°C for 7 hours, and distill off excess triethyl phosphite to obtain the phosphate salt; S2. Add the phosphate salt obtained in step S1 to the reaction vessel, dissolve it in 15 L of tetrahydrofuran, cool to 0°C, and add 1.3 kg of 60% sodium hydride in batches, stirring for 30 minutes to obtain Diethyl (2-oxopropyl)phosphonate.
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HS Code ]

29319090
[Storage Class]

10 - Combustible liquids
Hazard InformationBack Directory
[Chemical Properties]

CLEAR COLORLESS TO LIGHT YELLOW LIQUID
[Uses]

Diethyl (2-Oxopropyl)phosphonate, is used in the preparation of enantipure acetoxyalkanephosphonates thru dynamic enzymic kinetic resolution alpha- and beta-hydroxalkanephosphonates.
[Synthesis Reference(s)]

Tetrahedron, 34, p. 649, 1978 DOI: 10.1016/0040-4020(78)88099-5
Tetrahedron Letters, 17, p. 2829, 1976 DOI: 10.1016/S0040-4039(01)85513-1
[reaction suitability]

reaction type: C-C Bond Formation
Spectrum DetailBack Directory
[Spectrum Detail]

Diethyl (2-oxopropyl)phosphonate(1067-71-6)1HNMR
Diethyl (2-oxopropyl)phosphonate(1067-71-6)IR
Diethyl (2-oxopropyl)phosphonate(1067-71-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Diethyl (2-oxopropyl)phosphonate, 96%(1067-71-6)
[Alfa Aesar]

Diethyl acetylmethylphosphonate, 97%(1067-71-6)
[Sigma Aldrich]

1067-71-6(sigmaaldrich)
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