Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Aromatic ketones >  3-Benzyloxy acetophenone

3-Benzyloxy acetophenone

Basic information Safety Supplier Related

3-Benzyloxy acetophenone Basic information

Product Name:
3-Benzyloxy acetophenone
Synonyms:
  • m-benzyloxyacetophenone
  • 1-(3-Phenylmethoxyphenyl)ethanone
  • 1-[3-(BENZYLOXY)PHENYL]ETHAN-1-ONE
  • 1-(3-BENZYLOXYPHENYL)ETHANONE
  • 3-BENZYLOXYACETOPHENONE
  • ALPHA-BROMO-3'-BENZYLOXY ACETOPHENONE
  • 1-[3-(phenylmethoxy)phenyl]ethan-1-one
  • 3''-BENZYLOXYACETOPHENONE 97%
CAS:
34068-01-4
MF:
C15H14O2
MW:
226.27
EINECS:
251-816-0
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • Aromatics
Mol File:
34068-01-4.mol
More
Less

3-Benzyloxy acetophenone Chemical Properties

Melting point:
29-30 °C
Boiling point:
154°C/0.3mmHg(lit.)
Density 
1.0891 (rough estimate)
refractive index 
1.6530 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Low Melting Solid
color 
Light yellow
λmax
305nm(MeOH)(lit.)
CAS DataBase Reference
34068-01-4(CAS DataBase Reference)
More
Less

Safety Information

Safety Statements 
24/25
HS Code 
29145000

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
More
Less

3-Benzyloxy acetophenone Usage And Synthesis

Chemical Properties

Yellow Liquid

Synthesis

121-71-1

100-44-7

34068-01-4

Example 1 Synthesis of 3-benzyloxyacetophenone: 1 kg (7.35 mol) of 3-hydroxyacetophenone, 1.035 kg (7.5 mol) of anhydrous potassium carbonate, and 0.945 kg (7.5 mol) of benzyl chloride were dissolved in 4.1 L of acetone with mechanical stirring and heated and refluxed for 24 hrs. Subsequently, 0.1035 kg (0.75 mol) of anhydrous potassium carbonate and 0.0945 kg (0.75 mol) of benzyl chloride were added and refluxing was continued. the above additions were repeated after 72 hours and refluxing was continued to a total reaction time of 96 hours. After completion of the reaction, the reaction mixture was cooled, filtered and the filtrate was concentrated by rotary evaporator. To the concentrated filtrate was added 0.202 kg (2.0 mol) of triethylamine and stirred overnight. The reaction mixture was diluted with 1 L of ether and filtered, the filtrate was concentrated by evaporation and the residue was distilled to give 1.429 kg (86% yield) of the target product 3-benzyloxyacetophenone as an oil. Boiling point: 160°C (0.3 Torr).IR (CHCl3) spectrum showed absorption peaks located at 1695, 1605, 1595, 1493 and 1433 cm-1 .PMR (CDCl3) spectrum showed chemical shifts δ 2.52 (s, CH3), 5.03 (s, CH2) and 7.0-7.7 (m, Ph).

References

[1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988, p. 2491 - 2500
[2] Journal of Medicinal Chemistry, 1992, vol. 35, # 16, p. 3045 - 3049
[3] Tetrahedron Letters, 2007, vol. 48, # 26, p. 4627 - 4630
[4] Chemical and Pharmaceutical Bulletin, 1995, vol. 43, # 5, p. 738 - 747
[5] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 5, p. 1537 - 1544

3-Benzyloxy acetophenoneSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com