2-FLUORO-6-IODOBENZALDEHYDE
2-FLUORO-6-IODOBENZALDEHYDE Basic information
- Product Name:
- 2-FLUORO-6-IODOBENZALDEHYDE
- Synonyms:
-
- 2-
Fluoro- 6- iodobenzaldehyde - 2-Fluoro-6-iodobenzaldehyde97%
- 1-Fluoro-2-formyl-3-iodobenzene
- Benzaldehyde, 2-fluoro-6-iodo-
- 146137-72-6
- 2-
- CAS:
- 146137-72-6
- MF:
- C7H4FIO
- MW:
- 250.01
- Product Categories:
-
- Aryl Fluorinated Building Blocks
- Building Blocks
- Carbonyl Compounds
- Chemical Synthesis
- Fluorinated Building Blocks
- Organic Building Blocks
- Organic Fluorinated Building Blocks
- Other Fluorinated Organic Building Blocks
- Aromatic Aldehydes & Derivatives (substituted)
- Aldehydes
- C7
- Carbonyl Compounds
- Mol File:
- 146137-72-6.mol
2-FLUORO-6-IODOBENZALDEHYDE Chemical Properties
- Melting point:
- 36-40 °C
- Boiling point:
- 257.7±25.0 °C(Predicted)
- Density
- 1.962±0.06 g/cm3(Predicted)
- Flash point:
- 110 °C
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- form
- fused solid
- color
- Bright yellow liquid
2-FLUORO-6-IODOBENZALDEHYDE Usage And Synthesis
Chemical Properties
off-white crystalline
Synthesis
1121-86-4
68-12-2
146137-72-6
Procedure: 1. To a solution of 1-fluoro-3-iodobenzene (5.00 g, 22.5 mmol) in tetrahydrofuran (THF, 50 mL) was slowly added lithium diisopropylammonium (LDA, 17.0 mL, 33.7 mmol) dropwise at -78 °C. The reaction temperature was maintained at -78 °C for 2 hours. After maintaining the reaction temperature at -78 °C and stirring for 2 h, N,N-dimethylformamide (DMF, 4.90 g, 67.5 mmol) was added and stirring was continued at -78 °C for 30 min. 2. Upon completion of the reaction, the reaction was quenched with an aqueous ammonium chloride solution (20 mL) and water (30 mL), followed by extraction with ethyl ether (3 x 30 mL). The organic layers were combined, washed sequentially with 2N hydrochloric acid (20 mL) and saturated saline (20 mL), and dried over anhydrous sodium sulfate.3. The solvent was removed by pressure-relief concentration, and the resulting crude product was purified by column chromatography on silica gel, with the eluent being petroleum ether/ethyl acetate (100:1 to 50:1), to give 6-fluoro-2-iodobenzaldehyde (3.7 g, 66% yield). The product was characterized by 1H NMR (DMSO-d6, 500 MHz): δ10.01 (s, 1H), 7.89-7.79 (m, 1H), 7.44-7.40 (m, 2H).
References
[1] Patent: WO2013/41539, 2013, A1. Location in patent: Page/Page column 55; 56
[2] Patent: US2014/206702, 2014, A1. Location in patent: Paragraph 0277
[3] Chemistry - A European Journal, 2013, vol. 19, # 27, p. 8875 - 8883
[4] Tetrahedron Letters, 1992, vol. 33, # 49, p. 7499 - 7502
[5] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 12, p. 2998 - 3001
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