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4'-Bromo-3'-methylacetophenone

4'-Bromo-3'-methylacetophenone  Structure
CAS No.
37074-40-1
Chemical Name:
4'-Bromo-3'-methylacetophenone
Synonyms
NSC 405623;Fluralaner-003;Fluralaner Impurity 29;3-Methyl-4-bromoacetophenone;4'-Bromo-3'-methylacetophenone;4'-BROMO-3'-METHYLACETOPHENONE;Ethanone, 1-(4-broMo-3-Methylphenyl)-
CBNumber:
CB7947102
Molecular Formula:
C9H9BrO
Molecular Weight:
213.07
MOL File:
37074-40-1.mol
MSDS File:
SDS
Modify Date:
2024/5/8 9:18:20

4'-Bromo-3'-methylacetophenone Properties

Melting point 31-32 °C
Boiling point 157-159 °C(Press: 19 Torr)
Density 1.388±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form fused solid
color Pale lemon

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P271-P260-P280
HS Code  2914390090

4'-Bromo-3'-methylacetophenone Chemical Properties,Uses,Production

Uses

4'-Bromo-3'-methylacetophenone is a versatile building block that is used in the synthesis of many complex compounds. It can be used as a reactant, reagent, or speciality chemical.

Synthesis

A solution of 4-bromo-3-methylbenzaldehyde (4 g, 20 mmol) in dry tetrahydrofuran (40 mL) was cooled to 0??C under nitrogen atmosphere, and then methyl magnesium bromide (20 mL, 1N in tetrahydrofuran) was added dropwise. The ice bath was removed, and the mixture was stirred for 2 hours. Ammonium chloride aqueous (40 mL) was added and the mixture was extracted with dichloromethane (20 mL * 3). The organic phase was dried by sodium sulphate, filtered and concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate = 5:1) to give 1-(4-bromo-3-methylphenyl)ethanol. Colorless oil, yield 4.0 g, 93%. Pyridinium chlorochromate (48 g, 223 mmol) was added to a solution of 1-(4-bromo-3-methylphenyl)ethanol (31.9 g, 148 mmol) in dichloromethane (800 mL). The mixture was stirred at room temperature for 2 hours. The mixture was concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate = 25:1) to give 4'-Bromo-3'-methylacetophenone. Yield 27.3 g, 87%.
Synthesis_37074-40-1 Figure Synthesis of 4'-Bromo-3'-methylacetophenone

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Ethanone, 1-(4-broMo-3-Methylphenyl)- NSC 405623 3-Methyl-4-bromoacetophenone Fluralaner-003 4'-BROMO-3'-METHYLACETOPHENONE Fluralaner Impurity 29 4'-Bromo-3'-methylacetophenone 37074-40-1 Aromatic Acetophenones & Derivatives (substituted)