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4-Cyano-2-fluorobenzyl alcohol

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4-Cyano-2-fluorobenzyl alcohol Basic information

Product Name:
4-Cyano-2-fluorobenzyl alcohol
Synonyms:
  • 3-Fluoro-4-(hydroxymethyl)benzonitrile
  • Benzonitrile, 3-fluoro-4-(hydroxymethyl)- (9CI)
  • 4-Cyano-2-fluorobenzyl alcohol
  • 3-Fluoro-4-(hydroxyMethyl)-benzonitrile[4-cyano--2-fluorobenzyl alcohol
  • 3-Fluoro-4-(hydroxymethyl)benzonitrile99+%
  • Benzonitrile, 3-fluoro-4-(hydroxymethyl)-
  • 3-Fluoro-4-(hydroxymethyl)benzonitrile 97%
  • 4-Cyano-2-fluorobenzyl alcohol ISO 9001:2015 REACH
CAS:
219873-06-0
MF:
C8H6FNO
MW:
151.14
Product Categories:
  • HALIDE
  • ALDEHYDE
Mol File:
219873-06-0.mol
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4-Cyano-2-fluorobenzyl alcohol Chemical Properties

Melting point:
63-68°C
Boiling point:
288.8±30.0 °C(Predicted)
Density 
1.27 g/mL at 25 °C
storage temp. 
Sealed in dry,Room Temperature
pka
13.51±0.10(Predicted)
form 
crystalline powder
color 
Faint/pale lemon/gold
InChI
InChI=1S/C8H6FNO/c9-8-3-6(4-10)1-2-7(8)5-11/h1-3,11H,5H2
InChIKey
YGAURRAHPYQHDC-UHFFFAOYSA-N
SMILES
C(#N)C1=CC=C(CO)C(F)=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
WGK Germany 
1
HS Code 
2926907090
Storage Class
11 - Combustible Solids
Hazard Classifications
Eye Dam. 1
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4-Cyano-2-fluorobenzyl alcohol Usage And Synthesis

Uses

4-Cyano-2-fluorobenzyl alcohol is an essential drug intermediate and is widely applied to the synthesis of various drugs. For example: S1P1 Receptor agonists, drugs for treating Alzheimer's disease BMS708163, amides for treating arrhythmia, etc.

Synthesis

4-Cyano-2-fluorobenzyl alcohol, also known as 3-fluoro-4-hydroxymethylbenzonitrile, can be obtained by the reaction of 2-fluoro-4-bromobenzyl alcohol with zinc cyanide or by reduction of 4-cyano-2-fluorobenzoic acid methyl ester.

To a solution of 2-fluoro-4-bromobenzenemethanol (3.25 g, 15.85 mmol) in DMF (35 mL) was added zinc cyanide (1.85 g, 15.85 mmol), tetrakis(triphenylphosphine)palladium (Pd(PPh3) 4.0.916 g, 0.79 mmol), and the reaction was heated with argon deoxygenation for 16 hr. at 100 degrees C., cooled to Room temperature, diluted with ethyl acetate (100mL), washed by water (100mL??3), saturated brine (100mL??3), dried with anhydrous sodium sulfate and filtered, concentrated to crude, then purified by column chromatography (petroleum ether ~ ethyl acetate = 15/1 ~ 4/1 system elution) to obtain a white solid product (0.72g, yield 30%).

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