ChemicalBook--->CAS DataBase List--->70424-94-1

70424-94-1

70424-94-1 Structure

70424-94-1 Structure
IdentificationBack Directory
[Name]

METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE
[CAS]

70424-94-1
[Synonyms]

NSC 525276
METHYL TRIBENZYLGALLATE
Methyl Tri-O-benzylgallate
METHYL 3,4,5-TRIBENZYLOXYBENZOATE
METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE
methyl 3,4,5-tris(phenylmethoxy)benzoate
3,4,5-TRIBENZYLOXYBENZOIC ACID METHYL ESTER
3,4,5-TRIS(BENZYLOXY)BENZOIC ACID METHYL ESTER
3,4,5-Tris(phenylMethoxy)benzoic Acid Methyl Ester
Benzoic acid, 3,4,5-tris(phenylmethoxy)-, methyl ester
Methyl3,4,5-tris(benzyloxy)benzoateMethyl3,4,5-tris(benzyloxy)benzoate
Methyl 3,4,5-Tribenzyloxybenzoate 3,4,5-Tribenzyloxybenzoic Acid Methyl Ester 3,4,5-Tris(benzyloxy)benzoic Acid Methyl Ester
[Molecular Formula]

C29H26O5
[MDL Number]

MFCD03425302
[MOL File]

70424-94-1.mol
[Molecular Weight]

454.51
Chemical PropertiesBack Directory
[Melting point ]

98 °C
[Boiling point ]

584.5±40.0 °C(Predicted)
[density ]

1.191±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Acetone, Chloroform, Dichloromethane
[form ]

Solid
[color ]

White
[CAS DataBase Reference]

70424-94-1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2918.29.7500
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Intermediate in the production of Gallic Acid derivatives.
[Synthesis]

Methyl gallate

99-24-1

Benzyl bromide

100-39-0

METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE

70424-94-1

Benzyl bromide (4.4 g, 25.7 mmol) was added dropwise to a stirred solution of methyl 3,4,5-trihydroxybenzoate (0.94 g, 5.15 mmol) and potassium carbonate (6.56 g, 25.7 mmol) in N,N-dimethylformamide (DMF, 20 mL). The reaction mixture was stirred under nitrogen (N2) protection in an oil bath at 60 °C for 15 hours. Upon completion of the reaction, the reaction was quenched by adding an appropriate amount of water to the mixture and extracted with chloroform (3 × 20 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford methyl 3,4,5-tris(benzyloxy)benzoate (1.93 g, 90% yield) as a white solid.

[References]

[1] Patent: EP1870403, 2007, A1. Location in patent: Page/Page column 95
[2] Patent: US2004/110790, 2004, A1. Location in patent: Page 14
[3] Bioscience, Biotechnology and Biochemistry, 2003, vol. 67, # 12, p. 2584 - 2590
[4] Patent: US7288273, 2007, B1. Location in patent: Page/Page column 38
[5] Synthetic Communications, 2002, vol. 32, # 20, p. 3149 - 3158
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE(70424-94-1)1HNMR
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