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3-Fluorophenethyl alcohol

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3-Fluorophenethyl alcohol Basic information

Product Name:
3-Fluorophenethyl alcohol
Synonyms:
  • 3-Fluorophenethyl alcohol ,98%
  • 3-Fluorobenzeneethanol
  • 3-Fluorophenethyl alcohol,99%
  • 2-(3-Fluorophenyl)ethyl Alcohol 3-Fluorophenethyl Alcohol
  • 2-(3-Fluorophenyl)ethan-1-ol
  • 3-Fluorophenethylealcohol
  • 2-(3-FLUOROPHENYL)ETHANOL
  • 2-(M-FLUOROPHENYL)ETHANOL
CAS:
52059-53-7
MF:
C8H9FO
MW:
140.15
Product Categories:
  • Fluorine series
  • Oxygen Compounds
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
  • Alcohols
  • C7 to C8
Mol File:
52059-53-7.mol
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3-Fluorophenethyl alcohol Chemical Properties

Boiling point:
90 °C/3 mmHg (lit.)
Density 
1.125 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.509(lit.)
Flash point:
225 °F
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
pka
14.76±0.10(Predicted)
color 
Clear colorless
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Safety Information

Hazard Codes 
C,Xn
Risk Statements 
36/37/38-21/22-34
Safety Statements 
26-36/37/39-45-27
RIDADR 
2810
WGK Germany 
3
HS Code 
29062990

MSDS

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3-Fluorophenethyl alcohol Usage And Synthesis

Chemical Properties

clear colorless liquid

General Description

3-Fluorophenethyl alcohol is a fluorinated β-phenethyl alcohol. Regioselective synthesis of 3-fluorophenethyl alcohol via regioselective hydroboration has been reported.

Synthesis

331-25-9

52059-53-7

The general procedure for the synthesis of 3-fluorophenylethanol from 3-fluorophenylacetic acid was as follows: to a stirred solution of 3-fluorophenylacetic acid (5.0 g, 32.0 mmol) in ether (100 ml) was slowly added dropwise an ether solution of lithium aluminum hydroxide (32.4 ml, 1 M, 32.4 mmol) at -10 °C. The reaction mixture was gradually warmed to 25°C and stirred continuously for 1 hour. Subsequently, the reaction mixture was cooled again to -10°C and the reaction was quenched by sequential addition of methanol (20 ml) and 4M sodium hydroxide solution (20 ml). The resulting slurry was filtered and the filtrate was concentrated by evaporation under vacuum. The crude product was purified by silica gel column chromatography using CH2Cl2/MeOH/NH3 (80:8:1) as eluent to give 3-fluorophenylethanol (3.80 g, 84% yield) finally. The product was confirmed by NMR hydrogen spectrum (250 MHz, CDCl3): δ 2.87 (3H, t, J = 6.5 Hz, CH2), 3.87 (3H, t, J = 6.5 Hz, CH2), 6.89-7.02 (3H, m, Ar-H), 7.23-7.33 (1H, m, Ar-H).

References

[1] Journal of Organic Chemistry, 2005, vol. 70, # 14, p. 5528 - 5535
[2] Tetrahedron Asymmetry, 2001, vol. 12, # 4, p. 585 - 596
[3] Patent: US5889008, 1999, A
[4] Helvetica Chimica Acta, 1973, vol. 56, p. 2460 - 2479
[5] Journal of the American Chemical Society, 1978, vol. 100, p. 228 - 246

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