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ChemicalBook--->CAS DataBase List--->399-68-8

399-68-8

399-68-8 Structure

399-68-8 Structure
IdentificationMore
[Name]

4-Fluoroindole-2-carboxylic acid
[CAS]

399-68-8
[Synonyms]

4-FLUORO-1H-INDOLE-2-CARBOXYLIC ACID
4-FLUOROINDOLE-2-CARBOXYLIC ACID
INDOLE-2-CARBOXYLIC ACID, 4-FLUORO-
[Molecular Formula]

C9H6FNO2
[MDL Number]

MFCD02664471
[Molecular Weight]

179.15
[MOL File]

399-68-8.mol
Chemical PropertiesBack Directory
[Melting point ]

219-220 °C (decomp)
[Boiling point ]

422.2±25.0 °C(Predicted)
[density ]

1.510±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

powder
[pka]

4.32±0.30(Predicted)
[color ]

Pale yellow
[CAS DataBase Reference]

399-68-8(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P271
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Fluoroindole-2-carboxylic acid(399-68-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzenepropanoic acid, 4-fluoro-2-nitro-α-oxo-

7593-91-1

4-Fluoroindole-2-carboxylic acid

399-68-8

General procedure for the synthesis of 4-fluoroindole-2-carboxylic acid from the compound (CAS: 7593-91-1): 4.8 g (31 mmol) of compound 32 was dissolved in 60 mL of 4% NH4OH solution, which was subsequently added to a solution prepared from 52.45 g (188.7 mmol) of ferrous sulfate heptahydrate and 23 mL of concentrated NH4OH in 200 mL of water in a suspension of ferrous hydroxide. The reaction mixture was kept at boiling point for 5 minutes. Upon completion of the reaction, the resulting iron hydroxide precipitate was separated by filtration and washed repeatedly with dilute NH4OH and water. The filtrate was acidified with dilute HCl to a suitable pH and the precipitated solid was subsequently collected by filtration to afford 1.2 g (22% yield) of 4-fluoro-1H-indole-2-carboxylic acid (34) as a white solid. The resulting product could be used directly in the next step of the reaction without further purification.

[References]

[1] Journal of Medicinal Chemistry, 1988, vol. 31, # 5, p. 944 - 948
[2] Patent: US2014/66453, 2014, A1. Location in patent: Paragraph 0184-0185
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