Basic information Safety Supplier Related

4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER

Basic information Safety Supplier Related

4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER Basic information

Product Name:
4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER
Synonyms:
  • Benzoic acid, 4-(2-broMoacetyl)-, Methyl ester
  • Methyl 4-(BroMoacetyl)benzoate
  • Methyl p-(BroMoacetyl)benzoate
  • α-BroMo-4-(carboMethoxy)acetophenone
  • ω-BroMoacetophenone-4-carboxylic Αcid Methyl Ester
  • 4-(Methoxycarbonyl)phenacyl bromide, 2-Bromo-4'-(methoxycarbonyl)acetophenone
  • 4-(2-Bromoacetyl)benzoic acid methyl este
  • 4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER
CAS:
56893-25-5
MF:
C10H9BrO3
MW:
257.08
Product Categories:
  • Aromatics
  • Intermediates
Mol File:
56893-25-5.mol
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4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER Chemical Properties

Boiling point:
342.8±22.0 °C(Predicted)
Density 
1.494±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
Beige
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Safety Information

HS Code 
2917399590
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4-(2-BROMO-ACETYL)-BENZOIC ACID METHYL ESTER Usage And Synthesis

Uses

A phenacyl bromide

Synthesis

3609-53-8

56893-25-5

General procedure for the synthesis of methyl 4-(2-bromoacetyl)benzoate from methyl 4-acetylbenzoate: Bromine (2.71 mL, 52.5 mmol) was added dropwise to a solution of methyl 4-acetylbenzoate (8.91 g, 50.0 mmol) in acetic acid (80 mL). The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the mixture was cooled to 0 °C and filtered to collect the solid. The resulting precipitate was washed with a 1:1 mixed methanol-water solution and subsequently dried to afford methyl 4-(2-bromoacetyl)benzoate (10.6 g, 82% yield) as a brown solid. The product was characterized by 1H NMR (400 MHz, CDCl3) with chemical shifts of δ 8.19-8.12 (m, 2H), 8.04 (d, J = 8.5 Hz, 2H), 4.47 (s, 2H), 3.96 (s, 3H).

References

[1] Journal of the American Chemical Society, 2000, vol. 122, # 39, p. 9361 - 9366
[2] Patent: WO2006/78698, 2006, A1. Location in patent: Page/Page column 64
[3] Patent: US2012/196869, 2012, A1. Location in patent: Paragraph 0467; 0468; 0469
[4] Inorganic Chemistry, 2018, vol. 57, # 1, p. 120 - 128
[5] Patent: WO2008/33745, 2008, A2. Location in patent: Page/Page column 70-71

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