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22027-50-5

22027-50-5 Structure

22027-50-5 Structure
IdentificationMore
[Name]

Methyl 3-(4-methoxyphenyl)-3-oxopropionate
[CAS]

22027-50-5
[Synonyms]

3-(4-METHOXYPHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER
CBI-BB ZERO/004684
METHYL 4-METHOXYBENZOYLACETATE
4-methoxy-beta-oxo-benzenepropanoicacimethylester
methyl 3-(p-methoxyphenyl)-3-oxopropionate
EINECS 244-732-0
Methyl-3-(p-methoxyphenyl)-3-oxopropionat
METHYL 3-(4-METHOXYPHENYL)-3-OXOPROPANOATE
3-(4-Methoxyphenyl)-3-oxopropanoic acid methyl ester
Methyl 3-(4-methoxyphenyl)-3-oxopropionate
MTHYL4-METHOXYBENZOYLACETATE
METHY 4-METHOXYBENZOYLACETATE
3-Oxo-3-(4-methoxyphenyl)propanoic acid methyl ester
3-Oxo-3-(4-methoxyphenyl)propionic acid methyl ester
4-Methoxy-β-oxobenzenepropanoic acid methyl ester
β-Oxo-4-methoxybenzenepropanoic acid methyl ester
β-Oxo-4-methoxybenzenepropionic acid methyl ester
[EINECS(EC#)]

244-732-0
[Molecular Formula]

C11H12O4
[MDL Number]

MFCD01082033
[Molecular Weight]

208.21
[MOL File]

22027-50-5.mol
Chemical PropertiesBack Directory
[Melting point ]

40-42°C
[Boiling point ]

135°C/0.27mm
[density ]

1.147±0.06 g/cm3(Predicted)
[storage temp. ]

Store at room temperature
[pka]

10.31±0.25(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

22027-50-5(CAS DataBase Reference)
[EPA Substance Registry System]

22027-50-5(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Chemical Properties]

Pale yellow solid
[Synthesis]

Dimethyl carbonate

616-38-6

4'-Methoxyacetophenone

100-06-1

Methyl 3-(4-methoxyphenyl)-3-oxopropionate

22027-50-5

Step 1. A solution of p-methoxyacetophenone (30 g, 200 mmol, 1.00 eq.) was added to a 500-mL three-necked round-bottom flask. Sodium hydride (13.6 g, 340 mmol, 1.70 equiv, 60% dispersed in mineral oil) was added in batches. The reaction was stirred at 50 °C for 10 minutes. The reaction mixture was slowly poured into 400 mL of ice water and the resulting solution was washed with ether (50 mL x 2) and subsequently acidified with acetic acid. The aqueous phase was extracted with ethyl acetate (200 mL x 3) and the organic phases were combined. The organic phase was dried sequentially with saturated sodium bicarbonate solution and sodium sulfate. The organic phase was concentrated under reduced pressure to give 37 g (87% yield) of methyl 3-(4-methoxyphenyl)-3-oxopropionate as a yellow oil.

[References]

[1] Chemistry - A European Journal, 2017, vol. 23, # 41, p. 9716 - 9720
[2] Chemistry - A European Journal, 2018, vol. 24, # 32, p. 8092 - 8097
[3] Molecules, 2015, vol. 20, # 9, p. 17275 - 17287
[4] Synthesis (Germany), 2016, vol. 48, # 5, p. 772 - 782
[5] Angewandte Chemie - International Edition, 2017, vol. 56, # 43, p. 13319 - 13323
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-(4-methoxyphenyl)-3-oxopropionate(22027-50-5)1HNMR
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