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871101-87-0

871101-87-0 Structure

871101-87-0 Structure
IdentificationBack Directory
[Name]

1-(3-aMino-4-(benzyloxy)-2-hydroxyphenyl)ethanone
[CAS]

871101-87-0
[Synonyms]

1-(3-aMino-4-(benzyloxy)-2-hydroxyphenyl)ethanone
1-(3-amino-2-hydroxy-4-phenylmethoxyphenyl)ethanone
1-[3-amino-4-(benzyloxy)-2-hydroxyphenyl]ethan-1-one
Ethanone, 1-[3-amino-2-hydroxy-4-(phenylmethoxy)phenyl]-
[Molecular Formula]

C15H15NO3
[MDL Number]

MFCD20485008
[MOL File]

871101-87-0.mol
[Molecular Weight]

257.28
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

1-(4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone

1035229-31-2

1-(3-aMino-4-(benzyloxy)-2-hydroxyphenyl)ethanone

871101-87-0

The general procedure for the synthesis of 1-(3-amino-4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone from 1-(4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone was carried out as follows: zinc powder (5.50 g, 84.1 mmol) was added batchwise to 1-(4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone (5.50 g, 19.2 mmol) in a suspension in acetic acid (55 mL), and the reaction was carried out with an ice bath to control the internal temperature not to exceed 40 °C for 15 min. The reaction mixture was then warmed to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the mixture was filtered through diatomaceous earth and the filter cake was washed with acetic acid. The filtrate was slowly poured into an ice-water mixture (500 mL) and a solid was precipitated. The precipitate was collected by filtration, washed with water and dried under vacuum at 40 °C to afford the target product 1-(3-amino-4-(benzyloxy)-2-hydroxyphenyl)ethanone (4.80 g, 18.7 mmol, 97% yield) as a light brown solid. The mass spectrum (ESI+) showed the molecular ion peak m/z 258 [M + H]+.

[References]

[1] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 6, p. 695 - 700
[2] Patent: WO2008/75025, 2008, A1. Location in patent: Page/Page column 84-85
[3] Patent: US2016/31838, 2016, A1. Location in patent: Paragraph 0115
[4] Patent: WO2009/154557, 2009, A1. Location in patent: Page/Page column 32
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