ChemicalBook--->CAS DataBase List--->63057-72-7

63057-72-7

63057-72-7 Structure

63057-72-7 Structure
IdentificationBack Directory
[Name]

1-(BENZYLOXY)-4-BROMO-2-METHOXYBENZENE
[CAS]

63057-72-7
[Synonyms]

4-Bromo-2-methoxy-1-phenylmethoxybenzene
Benzene, 4-bromo-2-methoxy-1-(phenylmethoxy)-
[Molecular Formula]

C14H13BrO2
[MDL Number]

MFCD00092521
[MOL File]

63057-72-7.mol
[Molecular Weight]

293.16
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Spectrum DetailBack Directory
[Spectrum Detail]

1-(BENZYLOXY)-4-BROMO-2-METHOXYBENZENE(63057-72-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Bromo-2-methoxyphenol

7368-78-7

Benzyl bromide

100-39-0

1-(BENZYLOXY)-4-BROMO-2-METHOXYBENZENE

63057-72-7

Step 1: Synthesis of 1-(benzyloxy)-4-bromo-2-methoxybenzene (2). Potassium carbonate (K2CO3, 30.5 g, 221 mmol) and benzyl bromide (18.9 g, 171 mmol) were added to a solution of N,N-dimethylformamide (DMF, 150 mL) containing 4-bromo-2-methoxyphenol (15 g, 73.8 mmol). The reaction mixture was stirred at 100 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of water and the organic layer was extracted with ethyl acetate (EtOAc). The organic phases were combined and concentrated. The crude product was purified by column chromatography to afford the target compound 2 (17.6 g, 86% yield).

[References]

[1] Patent: US2005/43300, 2005, A1. Location in patent: Page/Page column 39
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 14, p. 2793 - 2799
[3] Journal of Organic Chemistry, 2002, vol. 67, # 10, p. 3425 - 3436
[4] Patent: WO2018/64557, 2018, A1. Location in patent: Paragraph 0444; 0445; 0446; 0447
[5] Patent: US2006/264473, 2006, A1. Location in patent: Page/Page column 5
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