DIETHYL DIMETHYLMALONATE
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
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
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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
DIETHYL DIMETHYLMALONATESupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- +86 (0) 571 85 58 67 18
- Tel
- 010-010-82967028 13522913783
- 2355560935@qq.com
DIETHYL DIMETHYLMALONATE(1619-62-1)Related Product Information
- 3-Ethoxy-2,2-dimethyl-3-oxopropanoic acid
- Diethyl 1,1-cyclobutanedicarboxylate
- DIETHYL DIETHYLMALONATE
- Diethyl 1,1-cyclopropanedicarboxylate
- Diethyl dibutylmalonate
- Diethyl dipropylmalonate
- DIETHYL DIMETHYLMALONATE
- BIS[(12-CROWN-4)METHYL] DODECYLMETHYLMALONATE
- Diethyl 2-ethyl-2-phenylmalonate
- Diethyl bis(hydroxymethyl)malonate
- Diethyl ethyl(isoamyl)malonate
- DIETHYL BIS(2-CYANOETHYL)MALONATE
- DIETHYL DIALLYLMALONATE
- 2-Methylpropanedioic acid
- Diethyl malonate
- Dimethylmalonic acid
- Diethyl methylmalonate
- Malonic acid