5-FLUORO-2-IODOBENZYL ALCOHOL
5-FLUORO-2-IODOBENZYL ALCOHOL Basic information
- Product Name:
- 5-FLUORO-2-IODOBENZYL ALCOHOL
- Synonyms:
-
- (5-Fluoro-2-iodophenyl)Methanol
- 5-Fluoro-2-iodobenzyl alcohol 97%
- (5-fluoro-2-iodophenyl)methano
- 5-Fluoro-2-iodobenzylalcohol97%
- (5-Fluoro-2-iodophenyl)
- Benzenemethanol, 5-fluoro-2-iodo-
- CAS:
- 877264-43-2
- MF:
- C7H6FIO
- MW:
- 252.02
- Mol File:
- 877264-43-2.mol
5-FLUORO-2-IODOBENZYL ALCOHOL Chemical Properties
- storage temp.
- 2-8°C(protect from light)
- Appearance
- White to off-white Solid
5-FLUORO-2-IODOBENZYL ALCOHOL Usage And Synthesis
Synthesis
52548-63-7
877264-43-2
Step 1: 5-fluoro-2-iodobenzoic acid (5.00 g, 18.80 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to 0 °C under nitrogen protection. The borane-dimethyl sulfide complex (3.57 mL, 37.60 mmol) was slowly added dropwise under stirring conditions, followed by gradual warming of the reaction mixture to room temperature. The reaction was stirred continuously for 16 hours at room temperature. Upon completion of the reaction, the mixture was carefully poured into ice and quenched by adding 10% aqueous potassium carbonate solution (50 mL). The mixture was extracted with dichloromethane (2 x 50 mL), the organic phases were combined, dried over magnesium sulfate and subsequently concentrated under reduced pressure to give 5-fluoro-2-iodobenzyl alcohol as a colorless solid (4.80 g, 91% yield).1H NMR (400 MHz, CDCl3): δ 7.68 (dd, 1H, J= Hz), 7.19 (dd, 1H, J= Hz), and 6.70 (td, 1H, J= Hz), 4.57 (d, 2H, J= Hz), 1.95 (t, 1H, J= Hz).
References
[1] Advanced Synthesis and Catalysis, 2015, vol. 357, # 14-15, p. 3206 - 3214
[2] Organic Letters, 2018, vol. 20, # 2, p. 345 - 348
[3] Patent: WO2013/132376, 2013, A1. Location in patent: Page/Page column 238
[4] Patent: US2006/52378, 2006, A1. Location in patent: Page/Page column 146
[5] Chemical Communications, 2013, vol. 49, # 31, p. 3254 - 3256
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