Basic information Safety Supplier Related

METHYL 4-BENZYLOXY-3-METHOXYBENZOATE

Basic information Safety Supplier Related

METHYL 4-BENZYLOXY-3-METHOXYBENZOATE Basic information

Product Name:
METHYL 4-BENZYLOXY-3-METHOXYBENZOATE
Synonyms:
  • METHYL BENZYL VANILLATE
  • METHYL 4-BENZYLOXY-3-METHOXYBENZOATE
  • RARECHEM AL BF 0064
  • 4-Benzyloxy-3-Methoxybenzoic Acid Methyl Ester
  • Benzoic acid, 3-Methoxy-4-(phenylMethoxy)-, Methyl ester
  • -3-methoxybenzoate
  • Methyl 4-(benzyloxy)
  • 3-?methoxy-?4-?(phenylmethoxy)?-?, methyl ester Benzoic acid
CAS:
56441-97-5
MF:
C16H16O4
MW:
272.3
Product Categories:
  • Aromatic Esters
Mol File:
56441-97-5.mol
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METHYL 4-BENZYLOXY-3-METHOXYBENZOATE Chemical Properties

Boiling point:
400.1±30.0 °C(Predicted)
Density 
1.153±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DCM, Ethyl Acetate
form 
Solid
color 
Off-White
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METHYL 4-BENZYLOXY-3-METHOXYBENZOATE Usage And Synthesis

Uses

4-Benzyloxy-3-methoxybenzoic Acid Methyl Ester is an intermediate in the synthesis of Clomiphene (C587025), an synthetic estrogen agonist-antagonist.

Synthesis

3943-74-6

100-39-0

56441-97-5

General method 1: 4-chloroquinazoline derivatives were synthesized as target products by the introduction of alkyl amino side chains. Specifically, this includes the preparation of 4-chloro-6-methoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazoline, 4-chloro-7-methoxy-6-[3-(4-methylpiperazin-1-yl)propoxy]quinazoline, and 4-chloro-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline. Step 1: Methyl vanillate or methyl isovanillate (7.29 g, 40 mmol) was dissolved in 25 mL of dimethylformamide, followed by the addition of potassium carbonate (8.29 g, 60 mmol) and benzyl bromide (5.26 mL, 44 mmol). The reaction mixture was heated to 100 °C and maintained at this temperature for 3 hours. After completion of the reaction, it was cooled to room temperature, diluted with water and the product was extracted several times with ethyl acetate. The organic phases were combined and washed sequentially with water and brine. The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to obtain methyl 4-benzyloxy-3-methoxybenzoate or methyl 3-benzyloxy-4-methoxybenzoate, and the product could be used for subsequent reaction without further purification.

References

[1] Patent: US2007/21446, 2007, A1. Location in patent: Page/Page column 14
[2] Patent: EP1785420, 2007, A1. Location in patent: Page/Page column 18
[3] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 18, p. 6728 - 6737
[4] Patent: EP1746096, 2007, A1. Location in patent: Page/Page column 23
[5] ChemMedChem, 2016, vol. 11, # 20, p. 2327 - 2338

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