ETHYL 4-METHOXY-3-OXO-BUTANOATE

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Products Intro: Product Name:ETHYL 4-METHOXY-3-OXO-BUTANOATE
CAS:66762-68-3
Purity:0.98 Package:1kg;50kg;100kg;1t
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Products Intro: Product Name:ETHYL 4-METHOXY-3-OXO-BUTANOATE
CAS:66762-68-3
Purity:95% Package:1KG;1USD
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CAS:66762-68-3
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:Ethyl 4-methoxy-3-oxobutanoate
CAS:66762-68-3
Purity:98% Package:As customer's requirement
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Products Intro: Product Name:Ethyl 4-methoxy-3-oxobutanoate
CAS:66762-68-3
Purity:0.95 Package:5kg;10kg;25kg

ETHYL 4-METHOXY-3-OXO-BUTANOATE manufacturers

ETHYL 4-METHOXY-3-OXO-BUTANOATE Basic information
Product Name:ETHYL 4-METHOXY-3-OXO-BUTANOATE
Synonyms:ETHYL 4-METHOXY-3-OXO-BUTANOATE;Ethyl 4-methoxy-3-oxobutanoate, Ethyl 4-methoxy-3-oxobutryate;Butanoic acid, 4-methoxy-3-oxo-, ethyl ester;4-Methoxy-3-oxo-butanoic acid ethyl ester;4-methoxy-acetoacetic acid ethyl ester;ETHYL 4-METHOXY-3-OXO-BUTANOATE ISO 9001:2015 REACH;ETHYL 4-METHOXYACETOACETATE;Ethyl 4-methoxy-3-oxobutanoate 98%
CAS:66762-68-3
MF:C7H12O4
MW:160.17
EINECS:
Product Categories:
Mol File:66762-68-3.mol
ETHYL 4-METHOXY-3-OXO-BUTANOATE Structure
ETHYL 4-METHOXY-3-OXO-BUTANOATE Chemical Properties
Boiling point 68-71 °C(Press: 5 Torr)
density 1.060±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka9.90±0.46(Predicted)
AppearanceColorless to light yellow Liquid
InChIInChI=1S/C7H12O4/c1-3-11-7(9)4-6(8)5-10-2/h3-5H2,1-2H3
InChIKeyCMKOJBYFNYDATH-UHFFFAOYSA-N
SMILESC(OCC)(=O)CC(=O)COC
Safety Information
HS Code 2918999090
MSDS Information
ETHYL 4-METHOXY-3-OXO-BUTANOATE Usage And Synthesis
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
ETHYL 4-METHOXY-3-OXO-BUTANOATE Preparation Products And Raw materials
Raw materialsBromine-->Sodium hydride-->Ethyl acetoacetate-->1,2-Dimethoxyethane-->Barium carbonate-->Methanol-->Ethyl 4-chloroacetoacetate-->N,N-Dimethylformamide
Preparation Products4(1H)-Pyrimidinone, 6-(methoxymethyl)- (9CI)
Tag:ETHYL 4-METHOXY-3-OXO-BUTANOATE(66762-68-3) Related Product Information
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