ChemicalBook--->CAS DataBase List--->883500-73-0

883500-73-0

883500-73-0 Structure

883500-73-0 Structure
IdentificationBack Directory
[Name]

5-bromo-7-fluoro-1H-indole
[CAS]

883500-73-0
[Synonyms]

5-Bromo-8-fluoroindole
5-bromo-7-fluoro-1H-indole
1H-Indole, 5-broMo-7-fluoro-
[Molecular Formula]

C8H5BrFN
[MDL Number]

MFCD04037876
[MOL File]

883500-73-0.mol
[Molecular Weight]

214.034
Chemical PropertiesBack Directory
[Melting point ]

28-32°C
[Boiling point ]

315.1±22.0 °C(Predicted)
[density ]

1.750±0.06 g/cm3(Predicted)
[Fp ]

>110℃
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

14.58±0.30(Predicted)
[Appearance]

white solid or yellow liquid
[InChI]

1S/C8H5BrFN/c9-6-3-5-1-2-11-8(5)7(10)4-6/h1-4,11H
[InChIKey]

TZRRRWOVYVGRSL-UHFFFAOYSA-N
[SMILES]

BrC1=CC2=C(NC=C2)C(F)=C1
Questions And AnswerBack Directory
[Uses]

5-Bromo-7-fluoroindole can be used as a pharmaceutical synthesis intermediate.
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-36/37/39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

5-bromo-7-fluoro-1H-indole(883500-73-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Fluoro-4-bromonitrobenzene

321-23-3

Vinylmagnesium bromide

1826-67-1

5-bromo-7-fluoro-1H-indole

883500-73-0

Vinylmagnesium bromide (1M solution in THF, 13.62 mL, 13.62 mmol) was added slowly and dropwise to a solution of 4-bromo-2-fluoro-1-nitrobenzene (1.0 g, 4.54 mmol) in tetrahydrofuran (THF, 20 mL) at -40 °C. The reaction mixture was stirred at this temperature for 60 minutes. Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous ammonium chloride (NH4Cl) and the mixture was extracted with ethyl acetate (EtOAc, 2 x 20 mL). The organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4) and concentrated to dryness under reduced pressure. Purification by fast column chromatography (silica gel, ethyl acetate: petroleum ether = 9:1) afforded 5-bromo-7-fluoro-1H-indole as a gel solid (0.24 g, 25% yield).

[References]

[1] European Journal of Organic Chemistry, 2006, # 13, p. 2956 - 2969
[2] Patent: US2012/252853, 2012, A1. Location in patent: Page/Page column 30
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