3-FLUORO-4-IODOTOLUENE
3-FLUORO-4-IODOTOLUENE Basic information
- Product Name:
- 3-FLUORO-4-IODOTOLUENE
- Synonyms:
-
- BUTTPARK 148\01-16
- 4-IODO-3-FLUOROTOLUENE
- 3-FLUORO-4-IODOTOLUENE
- Benzene, 2-fluoro-1-iodo-4-methyl-
- 3-FLUORO-4-IODOTOLUENE ISO 9001:2015 REACH
- CAS:
- 452-79-9
- MF:
- C7H6FI
- MW:
- 236.03
- Product Categories:
-
- Fluorine Compounds
- Iodine Compounds
- Aryl
- C7
- Halogenated Hydrocarbons
- Aromatic Halides (substituted)
- Halogen toluene
- Fluoro-contained Iodo series
- Mol File:
- 452-79-9.mol
3-FLUORO-4-IODOTOLUENE Chemical Properties
- Boiling point:
- 138-139 °C/9 mmHg (lit.)
- Density
- 1.803 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.5810(lit.)
- Flash point:
- 199 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- Appearance
- Pink to red Liquid
- Sensitive
- Light Sensitive
- CAS DataBase Reference
- 452-79-9(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 52/53
- Safety Statements
- 23-24/25-61-60
- WGK Germany
- 3
- Hazard Note
- Irritant
- HS Code
- 29039990
MSDS
- Language:English Provider:SigmaAldrich
3-FLUORO-4-IODOTOLUENE Usage And Synthesis
Chemical Properties
colorless to light yellow liqui
Synthesis
452-74-4
452-79-9
A solution was prepared by dissolving 4-bromo-3-fluorotoluene (10 g) in tetrahydrofuran (THF, 50 mL) under a dry nitrogen atmosphere and cooled to -72 °C. Subsequently, a hexane solution (35 mL) of 1.6 M n-butyllithium was slowly added at -72 °C, the reaction temperature was controlled not to exceed -65 °C and stirring was continued for 1 h at this temperature. A solution prepared by dissolving iodine (14.8 g) in THF (30 mL) was added to the above reaction mixture at -72 °C, ensuring that the internal temperature was not higher than -60 °C, after which it was slowly warmed to room temperature. Upon completion of the reaction, saturated aqueous ammonium chloride solution and hexane were added to the mixture to separate the organic layer. The organic layer was sequentially washed twice with 10% aqueous sodium sulfite, then with saturated brine and finally dried with anhydrous sodium sulfate. The desiccant was removed by filtration and the organic solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography to give 13.0 g of 3-fluoro-4-iodotoluene as a yellow liquid.
References
[1] Patent: US2014/275577, 2014, A1. Location in patent: Paragraph 0166; 0167
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3-FLUORO-4-IODOTOLUENE(452-79-9)Related Product Information
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- 2-FLUORO-6-IODOTOLUENE
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- 4-Iodotoluene
- 3-FLUORO-4-IODOBENZOTRIFLUORIDE
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