ChemicalBook--->CAS DataBase List--->54043-71-9

54043-71-9

54043-71-9 Structure

54043-71-9 Structure
IdentificationBack Directory
[Name]

4-methyl ester 2,2-dimethyl-Butanedioic acid
[CAS]

54043-71-9
[Synonyms]

2,2-Dimethylsuccinic acid 4-methyl ester
4-Methoxy-2,2-dimethyl-4-oxobutanoic acid
2,2-Dimethylbutanedioic acid 4-methyl ester
4-methyl ester 2,2-dimethyl-Butanedioic acid
Butanedioic acid, 2,2-dimethyl-, 4-methyl ester
[Molecular Formula]

C7H12O4
[MOL File]

54043-71-9.mol
[Molecular Weight]

160.17
Chemical PropertiesBack Directory
[Melting point ]

49-50℃
[Boiling point ]

256℃
[density ]

1.126
[Fp ]

101℃
[storage temp. ]

Store at room temperature
[pka]

4.50±0.28(Predicted)
[Appearance]

White to light yellow <49°C Solid,>50°C Liquid
Questions And AnswerBack Directory
[Uses]

4-Methoxy-2,2-dimethyl-4-oxobutanoic acid is a useful research chemical.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[HS Code ]

2917198090
Spectrum DetailBack Directory
[Spectrum Detail]

4-methyl ester 2,2-dimethyl-Butanedioic acid(54043-71-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

2,2-Dimethylsuccinic acid

597-43-3

4-methyl ester 2,2-dimethyl-Butanedioic acid

54043-71-9

General procedure for the synthesis of 4-methyl 2,2-dimethylbutanedioate from methanol and 2,2-dimethylsuccinic acid: Step 1. Preparation of 4-methoxy-2,2-dimethyl-4-oxobutanoic acid To a stirred solution of 2,2-dimethylsuccinic acid (4.5 g, 31 mmol) in methanol (45 mL) was added 98% H2SO4 (0.45 mL) dropwise at 0°C. The reaction mixture was then stirred at room temperature for 16 hours. Upon completion of the reaction, the solution was concentrated. To the residue was added saturated aqueous NaHCO3 solution (20 mL) and washed with hexane (50 mL x 3). The aqueous phase was then adjusted to pH=2 with 6N HCl, extracted with ethyl acetate (200 mL x 4), and the organic phase was dried with Na2SO4 and concentrated. 2,2-Dimethylbutanedioic acid 4-methyl ester (2.5 g, 51% yield) was obtained as a colorless oil without further purification. 1H NMR (500 MHz, CDCl3): δ 3.65 (s, 3H), 2.61 (s, 2H), 1.27 (s, 6H) ppm.

[References]

[1] Patent: WO2012/82436, 2012, A2. Location in patent: Page/Page column 275
[2] Patent: WO2014/12081, 2014, A2. Location in patent: Paragraph 0017; 00110
[3] Journal of the Chemical Society, 1904, vol. 85, p. 539
[4] Bulletin de la Societe Chimique de France, 1964, p. 828 - 830
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