4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester

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Products Intro: Product Name:4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester
CAS:656257-45-3
Purity:95% Package:1KG;1USD
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Products Intro: Product Name:4-(4-Ethylpiperazin-1-yl)phenylboronic acid pinacol ester
CAS:656257-45-3
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Products Intro: Product Name:1-ethyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine
CAS:656257-45-3
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Products Intro: Product Name:1-Ethyl-4-[4-(4.4.5.5-tetramethyl-1.3.2-dioxaborolan-2-yl)phenyl]piperazine
CAS:656257-45-3
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Products Intro: Product Name:4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester
CAS:656257-45-3
Purity:99% Package:1kg;25kg

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4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester Basic information
Product Name:4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester
Synonyms:4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester;1-Ethyl-4-[4-(4.4.5.5-tetraMethyl-1.3.2-dioxaborolan-2-yl)phenyl]piperazine;4-(4-Ethylpiperazino)phenylboronic Acid Pinacol Ester;4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpicolester;Piperazine, 1-ethyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
CAS:656257-45-3
MF:C18H29BN2O2
MW:316.25
EINECS:
Product Categories:
Mol File:656257-45-3.mol
4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester Structure
4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester Usage And Synthesis
Uses1-Ethyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine
Synthesis
Pinacolborane

25015-63-8

1-(4-BroMophenyl)-4-ethylpiperazine

656257-43-1

4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester

656257-45-3

1-(4-Bromophenyl)-4-ethylpiperazine (3 g, 11 mmol) and pinacolborane were dissolved in dioxane (100 mL) and then 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.8 g, 12 mmol), dichlorobis(triphenylphosphine)palladium(II) (0.392 g, 0.57 mmol) and triethylamine (4.65 g, 33 mmol). The reaction mixture was heated to reflux for 12 hours. After completion of the reaction, the mixture was poured into water and extracted with dichloromethane. The organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with dichloromethane/methanol (9/1, v/v) as eluent. 4-(4-Ethyl-1-piperazinyl)phenylboronic acid pinacol ester was obtained as a brown oil, which crystallized on standing (2 g, yield 55.48%), melting point 130-134°C.

References[1] Patent: WO2004/13134, 2004, A2. Location in patent: Page 27; 28
[2] Patent: WO2004/13135, 2004, A1. Location in patent: Page 49
4-(4-Ethylpiperazin-1-yl)-phenylboronicacidpinacolester Preparation Products And Raw materials
Raw materials2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane-->Pinacolborane-->1-(4-BroMophenyl)-4-ethylpiperazine-->Triethylamine-->1,4-Dioxane
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