1001911-63-2

  • Product Name(9-Phenyl-9h-carbazol-2-yl)boronic acid
  • Molecular FormulaC18 H14 BNO2
  • Molecular Weight287.1
  • Purity99%
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Product Details

Quick Details

  • CasNo: 1001911-63-2
  • Molecular Formula: C18 H14 BNO2
  • Purity: 99%

Top Purity (9-phenyl-9H-carbazol-2-yl)boronic acid 1001911-63-2 In Bulk Supply

  • Molecular Formula:C18 H14 BNO2
  • Molecular Weight:287.126
  • Boiling Point:466.0±51.0 °C(Predicted) 
  • PKA:8.91±0.30(Predicted) 
  • PSA:45.39000 
  • Density:1.20±0.1 g/cm3(Predicted) 
  • LogP:2.46350 

(9-phenyl-9H-carbazol-2-yl)boronic acid(Cas 1001911-63-2) Usage

Uses

(9-phenyl-9H-carbazol-2-yl)boronic acid can be used as an intermediate in organic synthesis, mainly used in laboratory research and development and in the process of chemical and pharmaceutical synthesis.

Synthesis

Sub 1-3-1 (6.4g, 20mmol) was dissolved in anhydrous Ether, lowering the temperature of the reaction to -78°C, n-BuLi (2.5M in hexane) (1.4g, 22mmol) was added dropwise slowly, and after, the reaction It was stirred for 30 minutes. After lowering the temperature of the reaction back to -78°C dropwise Triisopropyl borate (5.6g, 30mmol). Stirring at room temperature, diluted with water and it binds the 2N HCl. After completion of reaction, ethyl acetate and water, dried over MgSO4 and the organic layer was extracted and recrystallized silicagel column and the resulting organic material and then concentrated to a Sub 1-4-1 4.5g (yield: 78%) was obtained.

 

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1001911-63-2 Process route

4-Bromophenylboronic acid
5467-74-3

4-Bromophenylboronic acid

(9‐phenyl‐9H‐carbazol‐2‐yl)boronic acid
1001911-63-2

(9‐phenyl‐9H‐carbazol‐2‐yl)boronic acid

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / toluene / 4 h / 100 °C
2.1: triethyl phosphite / 6 h / 150 °C
3.1: caesium carbonate / copper(l) iodide / toluene / 50 °C
3.2: 14 h / Reflux
4.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C
4.2: 12 h / 20 °C
With n-butyllithium; sodium carbonate; caesium carbonate; triethyl phosphite; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; hexane; toluene;
 
Multi-step reaction with 4 steps
1.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / toluene / 4 h / 100 °C
2.1: triethyl phosphite / 6 h / 150 °C
3.1: caesium carbonate / copper(l) iodide / toluene / 50 °C
3.2: 14 h / Reflux
4.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C
4.2: 12 h
With n-butyllithium; sodium carbonate; caesium carbonate; triethyl phosphite; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; hexane; toluene;
 
4'-bromo-2-nitrobiphenyl
35450-34-1

4'-bromo-2-nitrobiphenyl

(9‐phenyl‐9H‐carbazol‐2‐yl)boronic acid
1001911-63-2

(9‐phenyl‐9H‐carbazol‐2‐yl)boronic acid

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1.1: triethyl phosphite / 6 h / 150 °C
2.1: caesium carbonate / copper(l) iodide / toluene / 50 °C
2.2: 14 h / Reflux
3.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C
3.2: 12 h / 20 °C
With n-butyllithium; caesium carbonate; triethyl phosphite; copper(l) iodide; In tetrahydrofuran; hexane; toluene;
 
Multi-step reaction with 3 steps
1.1: triethyl phosphite / 6 h / 150 °C
2.1: caesium carbonate / copper(l) iodide / toluene / 50 °C
2.2: 14 h / Reflux
3.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C
3.2: 12 h
With n-butyllithium; caesium carbonate; triethyl phosphite; copper(l) iodide; In tetrahydrofuran; hexane; toluene;
 
Multi-step reaction with 3 steps
1.1: triethyl phosphate / 7 h / 150 °C
2.1: potassium phosphate; ethylenediamine / 12 h / Reflux
3.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
3.2: 12 h / -78 - 20 °C
3.3: 20 °C
With potassium phosphate; n-butyllithium; triethyl phosphate; ethylenediamine; In tetrahydrofuran; hexane;
 

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