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1818-27-5

1818-27-5 Structure

1818-27-5 Structure
IdentificationBack Directory
[Name]

1-(2,4,5-Trihydroxyphenyl)ethanone
[CAS]

1818-27-5
[Synonyms]

acetophenone, 2,4,5-trihydroxy
1-(2,4,5-Trihydroxyphenyl)ethanone
1-(2,4,5-trihydroxyphenyl)ethan-1-one
Ethanone, 1-(2,4,5-trihydroxyphenyl)-
[Molecular Formula]

C8H8O4
[MOL File]

1818-27-5.mol
[Molecular Weight]

168.15
Chemical PropertiesBack Directory
[Melting point ]

200-202 °C
[Boiling point ]

404.3±30.0 °C(Predicted)
[density ]

1.446±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

7.81±0.23(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

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

Preparation by Fries rearrangement of 1,2,4-triacetoxy-benzene,
with aluminium chloride in nitrobenzene (30–43%)
with zinc chloride at 135–140° (49–53%)
with p-toluenesulfonic acid in refluxing tetrachloroethane or benzene or without solvent at 135–140° (60%).
[Synthesis]

1-(6-hydroxy-1,3-benzodioxol-5-yl)Ethanone

66003-50-7

1-(2,4,5-Trihydroxyphenyl)ethanone

1818-27-5

General procedure for the synthesis of 1-(2,4,5-trihydroxyphenyl)ethan-1-one from 1-(6-hydroxybenzo[D][1,3]dioxolan-5-yl)ethan-1-one: The compound 1-(6-hydroxybenzo[D][1,3]dioxolan-5-yl)ethan-1-one (4 g, 19.03 mmol) was dissolved in chlorobenzene (20 mL) at room temperature, and in a Trichlorosilane (6.6 g, 49.47 mmol) was slowly added dropwise under nitrogen protection. The reaction mixture was heated to reflux for 24 hours. Upon completion of the reaction, the chlorobenzene was removed by rotary evaporation. The residue was dissolved in 1 M hydrochloric acid (50 mL) and extracted with ethyl acetate. The extract was post-treated and purified by silica gel column chromatography to afford 1-(2,4,5-trihydroxyphenyl)ethanone (2.1 g, 12.7 mmol) as a pale yellow solid in 66.9% yield.

[References]

[1] Patent: CN107935982, 2018, A. Location in patent: Paragraph 0023; 0024
[2] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 13, p. 3872 - 3875
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