1-(2,4,5-trichlorophenyl)ethan-1-one

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Products Intro: Product Name:1-(2,4,5-trichlorophenyl)ethan-1-one
CAS:13061-28-4
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CAS:13061-28-4
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Products Intro: Product Name:1-(2,4,5-Trichlorophenyl)ethanone
CAS:13061-28-4
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1-(2,4,5-trichlorophenyl)ethan-1-one Basic information
Product Name:1-(2,4,5-trichlorophenyl)ethan-1-one
Synonyms:1-(2,4,5-trichlorophenyl)ethan-1-one;2',4',5'-Trichloroacetophenone;Einecs 235-954-9;1-(2,4,5-trichlorophenyl)ethanone;Ethanone,1-(2,4,5-trichlorophenyl)-;Ceftizoxime Impurity 34
CAS:13061-28-4
MF:C8H5Cl3O
MW:223.48
EINECS:235-954-9
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Mol File:13061-28-4.mol
1-(2,4,5-trichlorophenyl)ethan-1-one Structure
1-(2,4,5-trichlorophenyl)ethan-1-one Chemical Properties
storage temp. Sealed in dry,Room Temperature
form fused solid
color White
Safety Information
HS Code 2914790090
MSDS Information
1-(2,4,5-trichlorophenyl)ethan-1-one Usage And Synthesis
Synthesis
Acetyl chloride

75-36-5

1,2,4-Trichlorobenzene

120-82-1

1-(2,4,5-trichlorophenyl)ethan-1-one

13061-28-4

Acetyl chloride (11.8 g, 150 mmol) was slowly added dropwise to a stirred mixture of 1,2,4-trichlorobenzene (18.2 g, 100 mmol) and anhydrous aluminum trichloride (33.4 g, 250 mmol) at room temperature. The reaction mixture was then gradually heated to 120-125°C (oil bath heating) and the reaction was maintained at this temperature for 3 hours. Upon completion of the reaction, the resulting viscous mixture was carefully poured into ice water (125 mL) to quench the reaction, followed by extraction of the aqueous phase with dichloromethane (3 x 70 mL). The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and the solvent concentrated under reduced pressure. The residue was purified by distillation under reduced pressure to give a colorless liquid product which solidified to a solid after standing at room temperature. Yield: 15.6 g (82% yield); melting point: 43-45 °C, boiling point: 135 °C/6 mmHg (literature values: melting point 47 °C [29]; 44-46 °C [30]; 45.5-46 °C [31], boiling point 114-116 °C/2 mmHg [31]).

References[1] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2017, vol. 72, # 5, p. 369 - 375
[2] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1977, p. 1541 - 1544
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