ChemicalBook--->CAS DataBase List--->37555-99-0

37555-99-0

37555-99-0 Structure

37555-99-0 Structure
IdentificationBack Directory
[Name]

2-ETHOXY-MALONIC ACID DIETHYL ESTER
[CAS]

37555-99-0
[Synonyms]

Diethyl ethoxymalonate
diethyl 2-ethoxymalonate
2-Hydroxydiethyl Malonate
Diethyl ethoxypropanedioate
diethyl 2-ethoxypropanedioate
1,3-diethyl 2-ethoxypropanedioate
ethoxy-malonic acid diethyl ester
2-ETHOXY-MALONIC ACID DIETHYL ESTER
Ethoxypropanedioic acid diethyl ester
Propanedioic acid, 2-ethoxy-, 1,3-diethyl ester
[Molecular Formula]

C9H16O5
[MDL Number]

MFCD00087125
[MOL File]

37555-99-0.mol
[Molecular Weight]

204.22
Chemical PropertiesBack Directory
[Boiling point ]

261℃
[density ]

1.070
[Fp ]

108℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.29±0.46(Predicted)
[Appearance]

Colorless to light yellow Liquid
Questions And AnswerBack Directory
[Uses]

Diethyl ethoxymalonate is a hydroxyl malonic acid ester and a commonly used reagent in organic synthesis.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Bromine-->Carbon tetrachloride-->Sodium ethoxide-->Diethyl malonate-->Ethyl ethoxyacetate-->Diethyl oxalate-->Hydrochloric acid
[Preparation Products]

Lomefloxacin
Spectrum DetailBack Directory
[Spectrum Detail]

2-ETHOXY-MALONIC ACID DIETHYL ESTER(37555-99-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl ethoxyacetate

817-95-8

Diethyl oxalate

95-92-1

2-ETHOXY-MALONIC ACID DIETHYL ESTER

37555-99-0

Example 1: Scheme 4 Preparation of diethyl 2-ethoxy-malonate A mixture of diethyl oxalate (39.23 ml, 1.12 eq.) and ethyl 2-ethoxyacetate (34.95 ml, 1 eq.) was added dropwise to a slurry of sodium ethanolate (18.64 g, 1.07 eq.) in toluene (100 ml) at 45-50 °C. After the dropwise addition was completed, the reaction mixture was heated to 70-80°C and maintained for 2 hours. After completion of the reaction, the mixture was cooled and poured into 70 ml of 14% hydrochloric acid solution. The resulting mixture was extracted with ethyl acetate (EA), the organic layers were combined and washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 55.86 g (93.7% yield) of the target product diethyl 2-ethoxy-malonate.

[References]

[1] Patent: WO2011/80568, 2011, A2. Location in patent: Page/Page column 47-48
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