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trans-2-(4-Methylphenyl)vinylboronic ac&

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trans-2-(4-Methylphenyl)vinylboronic ac& manufacturers

trans-2-(4-Methylphenyl)vinylboronic ac& Basic information
Product Name:trans-2-(4-Methylphenyl)vinylboronic ac&
Synonyms:1-(4-Methylphenyl)-vinyl-2-boronic acid;(4-Methylstyryl)boronic acid;(E)-(4-Methylstyryl)boronic acid;trans-2-(4-Methylphenyl)vinylboronic acid 97%;TRANS-2-(4-METHYLPHENYL)VINYLBORONIC;Boronic acid, B-[(1E)-2-(4-methylphenyl)ethenyl]-;(E)-2-(4-methylphenyl)ethenyl]boronic acid;trans-2-(4-Methylphenyl)vinylboronic acid
CAS:72316-17-7
MF:C9H11BO2
MW:161.99
EINECS:
Product Categories:Alkenyl;Boronic Acids;Boronic Acids and Derivatives
Mol File:72316-17-7.mol
trans-2-(4-Methylphenyl)vinylboronic ac& Structure
trans-2-(4-Methylphenyl)vinylboronic ac& Chemical Properties
Melting point 169-175 °C(lit.)
Boiling point 330.9±45.0 °C(Predicted)
density 1.100±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka9.70±0.43(Predicted)
form solid
AppearanceWhite to off-white Solid
InChI1S/C9H11BO2/c1-8-2-4-9(5-3-8)6-7-10(11)12/h2-7,11-12H,1H3/b7-6+
InChIKeyJJOBVKVXRDHVRP-VOTSOKGWSA-N
SMILES[H]\C(B(O)O)=C(\[H])c1ccc(C)cc1
Safety Information
WGK Germany 3
HS Code 2931900090
Storage Class11 - Combustible Solids
MSDS Information
trans-2-(4-Methylphenyl)vinylboronic ac& Usage And Synthesis
General DescriptionContains varying amount of anhydride
Synthesis
4-Ethynyltoluene

766-97-2

CATECHOLBORANE

274-07-7

TRANS-2-(4-METHYLPHENYL)VINYLBORONIC AC&

72316-17-7

General procedure for the synthesis of trans-2-(4-tolyl)vinylboronic acid from 1-ethynyl-4-methylbenzene and catecholborane: 1-ethynyl-4-methylbenzene (0.50 mL, 3.94 mmol, 1.00 equiv) and catecholborane (0.50 mL, 4.73 mmol, 1.20 equiv) were dissolved in tetrahydrofuran (THF, 1.5 mL) , and the mixture was refluxed for 18 hours. After completion of the reaction, the solvent was removed by evaporation and water (1 mL) was added. The resulting suspension was stirred vigorously for 4 h at room temperature. The solid was collected by filtration and recrystallized with water. Subsequent filtration afforded (E)-2-(4-tolyl)vinylboronic acid (309.4 mg, 1.90 mmol, 48% yield) and dried under vacuum. The product was characterized by 1H NMR (400 MHz, DMSO-d6) and 13C NMR (101 MHz, DMSO-d6) with the following data: 1H NMR (DMSO-d6) δ 7.73 (s, 2H), 7.36 (d, J = 7.9 Hz, 2H), 7.18 (d, J = 7.9 Hz, 2H), 6.05 (d, J = 18.3 Hz, 1H), 2.31 (s, 3H); 13C NMR (DMSO-d6) δ 146.2, 138.4, 135.4, 129.8 (2C), 127.0 (2C), 21.3.

References[1] Patent: WO2016/198836, 2016, A1. Location in patent: Paragraph 00140
[2] Organic Letters, 2014, vol. 16, # 13, p. 3444 - 3447
trans-2-(4-Methylphenyl)vinylboronic ac& Preparation Products And Raw materials
Raw materials4-Ethynyltoluene-->Catecholborane
Preparation Products4-Methylcinnamic acid
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