| Identification | Back 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 |
| Hazard Information | Back Directory | [Synthesis]
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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