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3',4'-Difluoroacetophenone

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3',4'-Difluoroacetophenone Basic information

Product Name:
3',4'-Difluoroacetophenone
Synonyms:
  • 1-(3,4-Difluorophenyl)ethan-1-one
  • 1-(3,4-DIFLUORO-PHENYL)-ETHANONE
  • 3,4-DIFLUOROACETOPHENONE
  • OTAVA-BB BB7020410077
  • Ethanone, 1-(3,4-difluorophenyl)-
  • 3,4-Difluoroacetophenone,98%
  • 3',4'-Difluoro
  • 3',4'-Difluoroacetophenone 99%
CAS:
369-33-5
MF:
C8H6F2O
MW:
156.13
EINECS:
206-717-7
Product Categories:
  • Acetophenone Series
  • Aromatic Acetophenones & Derivatives (substituted)
  • ketone
  • Miscellaneous
  • Adehydes, Acetals & Ketones
  • Fluorine Compounds
  • C7 to C8
  • Carbonyl Compounds
  • Ketones
  • bc0001
Mol File:
369-33-5.mol
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3',4'-Difluoroacetophenone Chemical Properties

Melting point:
19-20 °C(lit.)
Boiling point:
94-95 °C13 mm Hg(lit.)
Density 
1.246 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.4916(lit.)
Flash point:
167 °F
storage temp. 
Sealed in dry,Room Temperature
form 
powder to lump to clear liquid
color 
White or Colorless to Light yellow
Specific Gravity
1.246
Water Solubility 
INSOLUBLE
BRN 
2206856
InChIKey
VWJSSJFLXRMYNV-UHFFFAOYSA-N
CAS DataBase Reference
369-33-5(CAS DataBase Reference)
NIST Chemistry Reference
3',4'-Difluoroacetophenone(369-33-5)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29147000

MSDS

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3',4'-Difluoroacetophenone Usage And Synthesis

Chemical Properties

clear yellowish liquid after melting

Uses

3′,4′-Difluoroacetophenone may be used in chemical synthesis.

Definition

ChEBI: 1-(3,4-Difluorophenyl)ethan-1-one is an aromatic ketone.

Synthesis

367-11-3

75-36-5

369-33-5

Anhydrous aluminum trichloride (117 g) was slowly added to a mixed solution of 1,2-difluorobenzene (50 g) with acetyl chloride (86 g) at room temperature. The formed slurry was heated to 30°C with continuous stirring. Upon completion of the reaction, the red reaction mixture was cooled to 20 °C and subsequently slowly poured into 800 g of ice-water mixture with continued stirring for 30 min. The organic phase was separated and the aqueous phase was extracted with dichloromethane (3 x 500 ml). All organic phases were combined and washed sequentially with water (2 x 500 ml), saturated sodium bicarbonate solution (2 x 500 ml) and 15% brine (2 x 500 ml), followed by drying with anhydrous sodium sulfate. The organic phases were concentrated to remove the solvent and finally distilled under reduced pressure to collect the fractions at 95 °C/13 mmHg to give 3',4'-difluoroacetophenone (51 g).

References

[1] Journal of Fluorine Chemistry, 1980, vol. 15, p. 245 - 252
[2] Journal of the Indian Chemical Society, 1982, vol. 59, # 2, p. 293 - 294
[3] Heterocycles, 1981, vol. 16, # 9, p. 1545 - 1553
[4] Journal of Medicinal Chemistry, 1979, vol. 22, # 11, p. 1385 - 1389
[5] Heterocycles, 1981, vol. 16, # 1, p. 71 - 76

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