METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE
METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE Basic information
- Product Name:
- METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE
- Synonyms:
-
- METHYL TRIBENZYLGALLATE
- METHYL 3,4,5-TRIBENZYLOXYBENZOATE
- METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE
- 3,4,5-TRIS(BENZYLOXY)BENZOIC ACID METHYL ESTER
- 3,4,5-TRIBENZYLOXYBENZOIC ACID METHYL ESTER
- methyl 3,4,5-tris(phenylmethoxy)benzoate
- 3,4,5-Tris(phenylMethoxy)benzoic Acid Methyl Ester
- Methyl Tri-O-benzylgallate
- CAS:
- 70424-94-1
- MF:
- C29H26O5
- MW:
- 454.51
- Product Categories:
-
- Building Blocks for Dendrimers
- Functional Materials
- Aromatics
- Intermediates
- Mol File:
- 70424-94-1.mol
METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE Chemical Properties
- 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
METHYL 3,4,5-TRIS(BENZYLOXY)BENZOATE Usage And Synthesis
Chemical Properties
White Solid
Uses
Intermediate in the production of Gallic Acid derivatives.
Synthesis
99-24-1
100-39-0
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
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