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2-Fluoro-4-hydroxybenzaldehyde

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2-Fluoro-4-hydroxybenzaldehyde Basic information

Product Name:
2-Fluoro-4-hydroxybenzaldehyde
Synonyms:
  • 2-FLUORO-4-HYDROXYBENZALDEHYDE
  • 2-FLURO-4-HYDROXYBENZALDEHYDE
  • 2-Fluoro-4-hydroxybenzaldehyde,98%
  • 3-Fluoro-4-formylphenol
  • Benzaldehyde, 2-fluoro-4-hydroxy-
  • 2-Fluoro-6-nitroacetophenone
CAS:
348-27-6
MF:
C7H5FO2
MW:
140.11
Product Categories:
  • Aromatic Aldehydes & Derivatives (substituted)
  • API intermediates
Mol File:
348-27-6.mol
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2-Fluoro-4-hydroxybenzaldehyde Chemical Properties

Melting point:
168-170°C
Boiling point:
254.2±20.0 °C(Predicted)
Density 
1.350±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
crystalline powder
pka
6.78±0.18(Predicted)
color 
Light tan
InChI
InChI=1S/C7H5FO2/c8-7-3-6(10)2-1-5(7)4-9/h1-4,10H
InChIKey
ONRPXRPUBXXCCM-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=C(O)C=C1F
CAS DataBase Reference
348-27-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41-52
Safety Statements 
26-39
Hazard Note 
Irritant
HS Code 
2912490090
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2-Fluoro-4-hydroxybenzaldehyde Usage And Synthesis

Uses

2-Fluoro-4-hydroxybenzaldehyde is a useful reagent for preparation of 3,4-ring fused 7-azaindoles and deazapurines as potent JAK2 inhibitors.

Uses

2-Fluoro-4-hydroxybenzaldehyde is mainly used as an intermediate for physiologically active compounds such as pharmaceuticals or pesticides and is a wide range of organic building blocks. Its structure contains fluorine, aldehyde groups, and phenolic hydroxyl groups, and these groups can add or replace other functional groups.

Synthesis

Preparation of 2-fluoro-4-hydroxybenzaldehyde involves: (1) mixing 3-fluorophenol (I), potassium carbonate, and 2-bromopropane in an organic solvent, and heating to react to obtain 1-fluoro-3-isopropoxybenzene (II); (2) dissolving compound (II) in an organic solvent and reacting with a brominating reagent to obtain 1-bromo-2-fluoro-4-isopropoxybenzene (III); (3) dissolving compound (III) in tetrahydrofuran, dripping isopropylmagnesium chloride/tetrahydrofuran solution at -10°C to 0°C, adding dimethylformamide to react after Grignard exchange to obtain 2-fluoro-4-isopropoxybenzaldehyde (IV); and (4) reacting compound (IV) with boron trichloride and deprotecting.

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