2-(3-Methoxy-5-trifluoromethyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane synthesis
- Product Name:2-(3-Methoxy-5-trifluoromethyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
- CAS Number:479411-93-3
- Molecular formula:C14H18BF3O3
- Molecular Weight:302.1
454-90-0
73183-34-3
479411-93-3
The general procedure for the synthesis of 2-(3-methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolanes from m-trifluoromethyl anisole and bis(pinacolato)boronic acid esters was as follows: to a flame-dried 100 mL Schlenk tube were added sequentially bis(pinacolato)diboron (350 mg, 1.38 mmol), [Ir( COD)Cl]2 (12 mg, 0.018 mmol), sodium methanol (5 mg, 0.09 mmol), and 4,4'-di-tert-butyl-2,2'-bipyridine (8 mg, 0.03 mmol). The flask was evacuated and filled with argon for protection, followed by the addition of 3-trifluoromethylanisole (2.5 mL). The flask was again evacuated (complete vacuum for 2 min), then sealed under vacuum and placed in a 90 °C oil bath for 96 h of reaction. Upon completion of the reaction, the reaction mixture was transferred to a round bottom flask using ethyl acetate and purified by Kugelrohr distillation. The resulting product was a viscous oil and was distilled at 120°C for 10 min. Final isolation gave 497 mg (1.65 mmol, 60% yield) of the target compound. The 1H NMR (400 MHz, CDCl3) data of the product were as follows: δ 7.62 (s, 1H), 7.43 (s, 1H), 7.18 (s, 1H), 3.82 (s, 3H), 1.32 (s, 12H).
454-90-0
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73183-34-3
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479411-93-3
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Yield:479411-93-3 100%
Reaction Conditions:
with [Ir(COD)(OMe)]2-Covalent organic framework (4-iPr) in n-heptane at 100; for 24 h;Inert atmosphere;Reagent/catalyst;
References:
Wu, Xiaowei;Han, Xing;Liu, Yuhao;Liu, Yan;Cui, Yong [Journal of the American Chemical Society,2018,vol. 140,# 47,p. 16124 - 16133] Location in patent:supporting information
454-90-0
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25015-63-8
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479411-93-3
37 suppliers
$30.00/1g