ChemicalBook--->CAS DataBase List--->23077-44-3

23077-44-3

23077-44-3 Structure

23077-44-3 Structure
IdentificationBack Directory
[Name]

6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID
[CAS]

23077-44-3
[Synonyms]

OTAVA-BB 1149596
RARECHEM AL BE 0955
UKRORGSYN-BB BBV-5127372
6-Fluoro-indole-3-carboxylic acid
Indole-3-carboxylic acid, 6-fluoro-
6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID
1H-Indole-3-carboxylic acid, 6-fluoro-
[Molecular Formula]

C9H6FNO2
[MDL Number]

MFCD06203359
[MOL File]

23077-44-3.mol
[Molecular Weight]

179.15
Chemical PropertiesBack Directory
[Melting point ]

242-244 °C (decomp)
[Boiling point ]

422.2±25.0 °C(Predicted)
[density ]

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

Inert atmosphere,Room Temperature
[pka]

3.73±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[RIDADR ]

UN2811
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID(23077-44-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Fluoroindole

399-51-9

Trifluoroacetic anhydride

407-25-0

6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID

23077-44-3

Trifluoroacetic anhydride (9.009 mL, 64.8 mmol, 2.2 eq.) was added slowly and dropwise to a stirred solution of 6-fluoroindole (4.000 g, 29.6 mmol, 1.0 eq.) dissolved in DMF (25 mL) at 0 °C (temperature controlled using an external ice bath). After the reaction mixture was kept in the ice bath for 3 h, the reaction was quenched with 40 mL of 2N sodium carbonate solution. The precipitate was collected by filtration and washed with distilled water. The resulting solid was dissolved in 4 M NaOH solution (50 mL) and refluxed for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and poured into 50 mL of distilled water. The mixture was cooled again in an ice bath and the pH was adjusted slowly by adding 6N HCl to 3. The precipitate precipitated was collected by filtration, washed with distilled water and dried under vacuum to give the off-white solid product 6-fluoro-1H-indole-3-carboxylic acid (3.5 g, 66% yield).

[References]

[1] Patent: WO2017/197177, 2017, A1. Location in patent: Paragraph 0219-0221
[2] ChemMedChem, 2012, vol. 7, # 11, p. 1915 - 1920
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