ChemicalBook--->CAS DataBase List--->66762-68-3

66762-68-3

66762-68-3 Structure

66762-68-3 Structure
IdentificationBack Directory
[Name]

ETHYL 4-METHOXY-3-OXO-BUTANOATE
[CAS]

66762-68-3
[Synonyms]

ETHYL 4-METHOXYACETOACETATE
ETHYL 4-METHOXY-3-OXO-BUTANOATE
4-methoxy-acetoacetic acid ethyl ester
4-Methoxy-3-oxo-butanoic acid ethyl ester
Butanoic acid, 4-methoxy-3-oxo-, ethyl ester
ETHYL 4-METHOXY-3-OXO-BUTANOATE ISO 9001:2015 REACH
Ethyl 4-methoxy-3-oxobutanoate, Ethyl 4-methoxy-3-oxobutryate
[Molecular Formula]

C7H12O4
[MDL Number]

MFCD07783018
[MOL File]

66762-68-3.mol
[Molecular Weight]

160.17
Chemical PropertiesBack Directory
[Boiling point ]

68-71 °C(Press: 5 Torr)
[density ]

1.060±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

9.90±0.46(Predicted)
[Appearance]

Colorless to light yellow Liquid
[InChI]

InChI=1S/C7H12O4/c1-3-11-7(9)4-6(8)5-10-2/h3-5H2,1-2H3
[InChIKey]

CMKOJBYFNYDATH-UHFFFAOYSA-N
[SMILES]

C(OCC)(=O)CC(=O)COC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P301+P312
[HS Code ]

2918999090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Bromine-->Sodium hydride-->Ethyl acetoacetate-->1,2-Dimethoxyethane-->Barium carbonate-->Methanol-->Ethyl 4-chloroacetoacetate-->N,N-Dimethylformamide
[Preparation Products]

4(1H)-Pyrimidinone, 6-(methoxymethyl)- (9CI)
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

Ethyl 4-chloroacetoacetate

638-07-3

ETHYL 4-METHOXY-3-OXO-BUTANOATE

66762-68-3

NaH (7.71 g, 192.7 mmol) was suspended in DMF (110 mL) and cooled to 0°C in an ice bath. A solution of MeOH (2.64 g, 82.5 mmol) in DMF (55 mL) was slowly added dropwise. After the dropwise addition, stirring was continued for 30 min at 0 °C. Subsequently, a DMF (55 mL) solution of ethyl 4-chloroacetoacetate (9.54 g, 57.9 mmol) was added slowly dropwise at 0 °C. After completion of the dropwise addition, the reaction mixture was slowly warmed to room temperature and stirred for 16 hours. After completion of the reaction, the reaction mixture was diluted with 1N HCl (400 mL) and extracted with MTBE (250 mL x 3). The organic phases were combined, washed with H2O (200 mL × 5), dried over anhydrous Na2SO4, filtered and concentrated. Finally, it was purified by silica gel column chromatography (eluent ratio PE:EA = 10:1) to afford ethyl 4-methoxy-3-oxobutanoate (1.4 g, 15.1% yield) as a light yellow oil.

[References]

[1] Patent: JP2015/214548, 2015, A. Location in patent: Paragraph 0992; 0993
[2] Patent: CN105481694, 2016, A. Location in patent: Paragraph 0015; 0016; 0017; 0018; 0019; 0020; 0021 - 0023
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