ChemicalBook--->CAS DataBase List--->18066-68-7

18066-68-7

18066-68-7 Structure

18066-68-7 Structure
IdentificationMore
[Name]

ETHYL 3,4-DIMETHOXYPHENYLACETATE
[CAS]

18066-68-7
[Synonyms]

ETHYL 2-(3,4-DIMETHOXYPHENYL)ACETATE
ETHYL 3,4-DIMETHOXYPHENYLACETATE
HOMOVERATRIC ACID ETHYL ESTER
3,4-dimethoxy-benzeneaceticaciethylester
Acetic acid, (3,4-dimethoxyphenyl)-, ethyl ester
Benzeneacetic acid, 3,4-dimethoxy-, ethyl ester
Ethyl dimethoxyphenylacetate
3,4-Dimethoxyphenylacetic acid ethyl ester~Ethyl homoveratrate
ethyl homoveratrate
Ethyl 3,4-dimethoxyphenylacetate, 98+%
3,4-Dimethoxybenzeneacetic acid ethyl ester
[EINECS(EC#)]

241-974-9
[Molecular Formula]

C12H16O4
[MDL Number]

MFCD00017272
[Molecular Weight]

224.25
[MOL File]

18066-68-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

191 °C
[density ]

1.084±0.06 g/cm3(Predicted)
[refractive index ]

1.5180
[Fp ]

159-160°C/4mm
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[color ]

Brown
[BRN ]

2697968
[CAS DataBase Reference]

18066-68-7(CAS DataBase Reference)
[EPA Substance Registry System]

Benzeneacetic acid, 3,4-dimethoxy-, ethyl ester (18066-68-7)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[TSCA ]

Yes
[HS Code ]

2915390090
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 3,4-DIMETHOXYPHENYLACETATE(18066-68-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Ethyl 2-(3,4-dimethoxyphenyl)acetate, 97%(18066-68-7)
[Alfa Aesar]

Ethyl 3,4-dimethoxyphenylacetate, 98%(18066-68-7)
Hazard InformationBack Directory
[Synthesis]

(3,4-Dimethoxyphenyl)acetic acid

93-40-3

Ethanol

64-17-5

ETHYL 3,4-DIMETHOXYPHENYLACETATE

18066-68-7

In a typical reaction, 3,4-dimethoxyphenylacetic acid (332 g, 0.6 mol), ethanol (1.5-2 mol), and AMA 2:3 were mixed in a provided reaction glass tube equipped with a screw cap and magnetic stirrer until a wet mixture was formed. The reaction mixture was placed in a microwave reactor (Anton Parr Monowave 300) and irradiated at 80°C for 8 min or 120°C for 20 min. Upon completion of the reaction, the mixture was cooled, diluted with dichloromethane (41 mL), filtered by gravity and the filtrate was washed with dichloromethane. Subsequently, the filtrate was washed with saturated sodium carbonate solution and water. The organic layer was separated, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give ethyl 3,4-dimethoxyphenylacetate.

[References]

[1] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 4, p. 1586 - 1605
[2] Journal of Organic Chemistry, 2003, vol. 68, # 3, p. 1165 - 1167
[3] Synthetic Communications, 2014, vol. 44, # 16, p. 2386 - 2392
[4] Journal of Organic Chemistry, 2010, vol. 75, # 19, p. 6549 - 6562
[5] Tetrahedron, 1997, vol. 53, # 30, p. 10555 - 10564
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18066-68-7 93-40-3