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(S)-1-(2-FLUOROPHENYL)ETHANOL

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(S)-1-(2-FLUOROPHENYL)ETHANOL Basic information

Product Name:
(S)-1-(2-FLUOROPHENYL)ETHANOL
Synonyms:
  • (S)-2'-Fluorophenylethan-1-ol
  • (1S)-1-(2-Fluorophenyl)ethan-1-ol
  • (S)-2-Fluoro-alpha-methylbenzyl alcohol
  • (S)-1-(2-FLUOROPHENYL)ETHANOL
  • S-OF-PEL
  • (1S)-1-(2-Fluorophenyl)ethanol
  • (alphaS)-2-Fluoro-alpha-methylbenzenemethanol
  • (S)-1-(o-Fluorophenyl)ethanol
CAS:
171032-87-4
MF:
C8H9FO
MW:
140.15
Product Categories:
  • HALIDE
  • Alcohols, Hydroxy Esters and Derivatives
  • Chiral Compounds
Mol File:
171032-87-4.mol
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(S)-1-(2-FLUOROPHENYL)ETHANOL Chemical Properties

Boiling point:
193℃
Density 
1.123
Flash point:
88℃
storage temp. 
Sealed in dry,Room Temperature
pka
13.95±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2906290090
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(S)-1-(2-FLUOROPHENYL)ETHANOL Usage And Synthesis

Uses

(S)?-?1-?(2-?Fluorophenyl)?ethanol is a building block used in organic synthesis such as JN403, a novel nicotinic acetylcholine receptor α7 agonist.

Synthesis

445-27-2

171032-87-4

General procedure for the synthesis of (S)-1-(2-fluorophenyl)ethanol from o-fluoroacetophenone: (R)-methyloxazole borane (0.32 g, 1.2 mmol) was dissolved in tert-butanol (60 mL) under the protection of nitrogen, N,N-diethylanilinoborane (2.6 g, 16 mmol) was added followed by a slow, titrative addition of 1-(2-fluorophenyl)ethanone at 45 °C ( 2.0 g, 14 mmol) in tert-butanol solution (150 mL) and the reaction mixture was stirred. After 1 hour of reaction, the mixture was cooled to room temperature, methanol was added and concentrated. To the concentrate, 1.0 N hydrochloric acid was added and extracted with ethyl acetate, the organic layer was washed with saturated brine and dried with anhydrous sodium sulfate sequentially, and concentrated to obtain the crude product. The crude product was purified by silica gel column chromatography (eluent: hexane to hexane/ethyl acetate=85/15) to afford the title compound (S)-1-(2-fluorophenyl)ethanol (1.9 g, 92% yield) as a colorless liquid.1H-NMR (400 MHz, CDCl3) δ: 1.52 (3H, d, J=6.8 Hz), 5.17-5.24 (1H, m ), 6.98-7.05 (1H, m), 7.15 (1H, ddd, J=1.2, 7.6, 7.6 Hz), 7.21-7.28 (1H, m), 7.49 (1H, ddd, J=1.6, 7.6, 7.6 Hz).

References

[1] Journal of the American Chemical Society, 1998, vol. 120, # 51, p. 13529 - 13530
[2] Tetrahedron: Asymmetry, 2003, vol. 14, # 6, p. 710 - 716
[3] Patent: US2018/162868, 2018, A1. Location in patent: Paragraph 1572-1573
[4] Tetrahedron Asymmetry, 2002, vol. 13, # 13, p. 1347 - 1349
[5] Tetrahedron Letters, 2006, vol. 47, # 27, p. 4619 - 4622

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