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ChemicalBook CAS DataBase List 3-(4-Chlorophenyl)-9-phenyl-9H-carbazole
1026033-57-7

3-(4-Chlorophenyl)-9-phenyl-9H-carbazole synthesis

3synthesis methods
854952-58-2 Synthesis
9-Phenyl-9H-carbazol-3-ylboronic acid

854952-58-2
292 suppliers
$18.50/250mg

 3-(4-Chlorophenyl)-9-phenyl-9H-carbazole

1026033-57-7
21 suppliers
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Yield:1026033-57-7 97%

Reaction Conditions:

with tetrakis(triphenylphosphine) palladium(0);potassium carbonate in tetrahydrofuran;water at 80; for 8 h;Inert atmosphere;Reflux;

Steps:

1.1 Synthesis Example 1: Synthesis of intermediate I-1

In nitrogen 9-phenyl-9H-carbazol-3-ylboronic acid (100 g, 348 mmol) of tetrahydrofuran (THF) 0. 9 L senses a rotation velocity of the disk to, herein 1-bromo-4-chlorobenzene (73. 3 g, 383 mmol) and tetrakis (triphenylphosphine) palladium (4. 02 g, 3. 48 mmol) visitor is checked through a and agitating an alcohol is put into a container. Potassuim carbonate saturated in water (128 g, 870 mmol) in 80 °C doesn't have any error frames, the reflux by heating at a 8. Complete after reaction solution at a water doesn't have any error frames, then dichloromethane (DCM) extraction of water to the MgSO4 anhydride after triggers number, filter and was, concentrating it under reduced pressure. Thus-obtained residue number intermediate that is forward separated into flash column chromatography I-1 (119 g, 97%) is obtained

References:

KR2016/91198,2016,A Location in patent:Paragraph 0191