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| | 2-Ethoxycarbonylvinylboronic acid pinacol ester Basic information |
| Product Name: | 2-Ethoxycarbonylvinylboronic acid pinacol ester | | Synonyms: | Ethyl (2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate;[(E)-2-(Ethoxycarbonyl)vinyl]boronic acid, pinacol ester 95+%;ANICHEM-2038;(E)-ethyl 3-(hydroxy(3-hydroxy-2,3-diMethylbutan-2-yloxy)boryl)acrylate;[(E)-2-(Ethoxycarbonyl)vinyl]boronic acid, pinacol ester;Ethyl (2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-enoate, Ethyl (E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate, [(E)-2-(Ethoxycarbonyl)ethenyl]boronic acid, pinacol ester;2-ethoxylcarbonylvinyl boronic ester;[(E)-2-(Ethoxycarbonyl)vinyl]boronic acid, pinacol ester, pinacol ester | | CAS: | 1009307-13-4 | | MF: | C11H19BO4 | | MW: | 226.08 | | EINECS: | | | Product Categories: | Organoborons;Organic boronic acid | | Mol File: | 1009307-13-4.mol |  |
| | 2-Ethoxycarbonylvinylboronic acid pinacol ester Chemical Properties |
| Boiling point | 236.8±42.0 °C(Predicted) | | density | 1.01±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | liquid | | color | Clear, colourless |
| | 2-Ethoxycarbonylvinylboronic acid pinacol ester Usage And Synthesis |
| Uses | 2-Ethoxycarbonylvinylboronic acid pinacol ester is used in the synthesis of drugs and speciality organic chemicals. | | Synthesis | General procedure for the synthesis of (E)-2-(ethoxycarbonyl)vinylboronic acid pinacol ester from pinacol ester of bis(boronic acid) and ethyl propiolate: CuCl (1.5 mg, 0.015 mmol), NaOt-Bu (2.9 mg, 0.03 mmol) and Xantphos ligand (8.7 mg, 0.015 mmol) were placed in a nitrogen protected and THF (0.45 mL) treated oven-dried Schlenk tubes. A solution of bis(pinacolato)diboron (127 mg, 0.5 mmol) in THF (0.3 mL) was added to the reaction mixture, followed by stirring for 30 min at room temperature. Next, α,β-alkyne genistein (0.5 mmol) and MeOH (40 μL, 1 mmol) were added. The reaction tube was washed with additional THF (0.2 mL), sealed and stirring was continued until complete consumption of the starting material was confirmed by TLC detection. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and concentrated. Finally, the target product was purified by silica gel column chromatography. | | References | [1] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8903 - 8925,23
[2] Organic and Biomolecular Chemistry, 2015, vol. 13, # 26, p. 7136 - 7139
[3] New Journal of Chemistry, 2018, vol. 42, # 21, p. 17346 - 17350
[4] Chemical Communications, 2008, # 6, p. 733 - 734
[5] Tetrahedron, 2012, vol. 68, # 17, p. 3444 - 3449 |
| | 2-Ethoxycarbonylvinylboronic acid pinacol ester Preparation Products And Raw materials |
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