ChemicalBook--->CAS DataBase List--->6274-50-6

6274-50-6

6274-50-6 Structure

6274-50-6 Structure
IdentificationBack Directory
[Name]

2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester
[CAS]

6274-50-6
[Synonyms]

Methyl 2-(4-Methoxyphenyl)-2-Methylpropanoate
2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester
Benzeneacetic acid, 4-methoxy-α,α-dimethyl-, methyl ester
[Molecular Formula]

C12H16O3
[MDL Number]

MFCD19441873
[MOL File]

6274-50-6.mol
[Molecular Weight]

208.25
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Hazard InformationBack Directory
[Synthesis]

METHYL 4-METHOXYPHENYLACETATE

23786-14-3

Iodomethane

74-88-4

2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester

6274-50-6

Methyl iodomethane (23.64 g, 166.5 mmol) was added slowly and dropwise to a tetrahydrofuran (THF, 100 mL) solution of methyl 2-(4-methoxyphenyl)acetate (10.0 g, 55.49 mmol) at -78 °C. Subsequently, potassium tert-butoxide (KOt-Bu, 18.68 g, 166.5 mmol) was added in batches over 30 min, keeping the reaction mixture stirred at -78 °C for 1 h. The reaction was then brought to room temperature and continued to be stirred for 1 h. The reaction was completed by the addition of potassium tert-butoxide (KOt-Bu, 18.68 g, 166.5 mmol). Upon completion of the reaction, the reaction was quenched by the addition of water (25 mL) and extracted with ethyl acetate (EtOAc, 2 x 250 mL). The organic layers were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give methyl 2-(4-methoxyphenyl)-2-methylpropionate (10.46 g, 91% yield).

[References]

[1] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 87
[2] Patent: WO2013/19635, 2013, A1. Location in patent: Page/Page column 55
[3] Helvetica Chimica Acta, 1971, vol. 54, p. 868 - 897
[4] Biomedical mass spectrometry, 1976, vol. 3, # 6, p. 316 - 328
[5] Patent: US5776951, 1998, A
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