ChemicalBook--->CAS DataBase List--->3044-06-2

3044-06-2

3044-06-2 Structure

3044-06-2 Structure
IdentificationBack Directory
[Name]

(1-Ethoxyethylidene)propanedioic acid diethyl ester
[CAS]

3044-06-2
[Synonyms]

100574
Nsc 233875
Einecs 221-249-3
diethyl 2-(1-ethoxyethylidene)Malonate
Diethyl (1-ethoxyethylidene)malonate 97%
diethyl 2-(1-ethoxyethylidene)propanedioate
Malonic acid, (1-ethoxyethylidene)-, diethyl ester
(1-Ethoxyethylidene)propanedioic acid diethyl ester
Propanedioic acid, (1-ethoxyethylidene)-, diethyl ester
Propanedioic acid, 2-(1-ethoxyethylidene)-, 1,3-diethyl ester
[EINECS(EC#)]

221-249-3
[Molecular Formula]

C11H18O5
[MDL Number]

MFCD22575006
[MOL File]

3044-06-2.mol
[Molecular Weight]

230.26
Chemical PropertiesBack Directory
[Melting point ]

26-27℃
[Boiling point ]

123-128℃ (3 Torr)
[density ]

1.068 g/cm3(Temp: 25 °C)
[refractive index ]

1.4634 (589.3 nm 25℃)
[storage temp. ]

Sealed in dry,2-8°C
[Appearance]

Colorless to light yellow <25°C Solid,>27°C Liquid
[InChI]

InChI=1S/C11H18O5/c1-5-14-8(4)9(10(12)15-6-2)11(13)16-7-3/h5-7H2,1-4H3
[InChIKey]

TWYCKMOLLPVQMA-UHFFFAOYSA-N
[SMILES]

C(OCC)(=O)/C(=C(/OCC)\C)/C(OCC)=O
[EPA Substance Registry System]

Propanedioic acid, (1-ethoxyethylidene)-, diethyl ester (3044-06-2)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H302-H319
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[TSCA ]

TSCA listed
[HS Code ]

2917198090
Spectrum DetailBack Directory
[Spectrum Detail]

(1-Ethoxyethylidene)propanedioic acid diethyl ester(3044-06-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Diethyl acetylmalonate

570-08-1

Triethyl orthoacetate

78-39-7

(1-Ethoxyethylidene)propanedioic acid diethyl ester

3044-06-2

a) Synthesis of diethyl 2-(1-ethoxyethylidene) malonate. A mixture of diethyl acetylmalonate (10 g, 0.049 mol), triethyl orthoacetate (24 g, 0.15 mol) and zinc chloride (70 mg, 0.0049 mol) was stirred and reacted at 95 °C for 4 h under inert atmosphere. After completion of the reaction, the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether=10:90) to afford the target product diethyl 2-(1-ethoxyethylidene)malonate as an oil (6.4 g, 56% yield). The product was analyzed by LC/MS: MS (ES+) m/e 231 (MH+); 1H NMR (300 MHz, CDCl3) δppm 1.22-1.33 (m, 9H), 2.43 (s, 3H), 4.06 (q, J=6.9 Hz, 2H), 4.16 (q, J=7.2 Hz, 2H), 4.26 (q, J=7.2 Hz, 2H).

[References]

[1] Patent: WO2013/96153, 2013, A1. Location in patent: Page/Page column 162
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