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DIETHYL DIMETHYLMALONATE

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DIETHYL DIMETHYLMALONATE Basic information

Product Name:
DIETHYL DIMETHYLMALONATE
Synonyms:
  • 2,2-dimethyl-malonicaciddiethylester
  • Diethyl 2,2-dimethylmalonate
  • Malonic acid, dimethyl-, diethyl ester
  • DIETHYL DIMETHYLMALONATE
  • Dimethylmalonic Acid Diethyl Ester
  • 2,2-Dimethylpropanedioic acid diethyl ester
  • Diethyl dimethylmalonate,97%
  • Propanedioic acid, 2,2-diMethyl-, 1,3-diethyl ester
CAS:
1619-62-1
MF:
C9H16O4
MW:
188.22
EINECS:
216-582-6
Product Categories:
  • C8 to C9
  • Carbonyl Compounds
  • Esters
  • Pharmaceutical Intermediates
Mol File:
1619-62-1.mol
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DIETHYL DIMETHYLMALONATE Chemical Properties

Melting point:
-30.4°C
Boiling point:
192 °C (lit.)
Density 
0.991 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.412(lit.)
Flash point:
160 °F
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
color 
Clear colorless
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-52/53
Safety Statements 
24/25-61
WGK Germany 
3
HS Code 
29171900

MSDS

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DIETHYL DIMETHYLMALONATE Usage And Synthesis

Chemical Properties

CLEAR COLOURLESS LIQUID

General Description

Diethyl dimethylmalonate forms adducts with α,α,α′,α′-tetraaryl-1,3-dioxolane-4,5-dimethanol based titanium catalysts.

Synthesis

105-53-3

74-88-4

1619-62-1

1) Synthesis of diethyl 2,2-dimethylmalonate (Compound 1-2): Dissolve sodium (36 g, 1.56 mol) in 800 mL of anhydrous ethanol and cool in an ice water bath. Slowly add diethyl malonate (compound 1-1) (100 g, 0.62 mol) dropwise. After completion of the dropwise addition, continue the slow dropwise addition of iodomethane (97.3 mL, 1.56 mol). After completion of the dropwise addition, the ice water bath was removed and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, 1000 mL of water was added to the mixture and extracted three times with 1000 mL of ethyl acetate. The organic phases were combined, washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The desiccant was removed by filtration and the filtrate was concentrated to give the crude product Compound 1-2 as a light yellow oil (102.1 g, 87.5% yield), which could be used in the next reaction without further purification.

References

[1] Molecules, 2016, vol. 21, # 5,
[2] Patent: US2014/179638, 2014, A1. Location in patent: Page/Page column
[3] Synthesis, 1985, # 1, p. 54 - 55
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1992, # 3, p. 365 - 368
[5] Patent: WO2015/95227, 2015, A2. Location in patent: Page/Page column 101

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