Benzofuran-2-boronic acid
Benzofuran-2-boronic acid Basic information
- Product Name:
- Benzofuran-2-boronic acid
- Synonyms:
-
- 1-BENZOFURAN-2-YLBORONIC ACID
- 2-BENZOFURANBORONIC ACID
- 2,3-BENZOBFURAN-2-BORONIC ACID
- AKOS BRN-0027
- BENZOFURAN-2-BORONIC ACID
- BENZOFURAN-2-YLBORONIC ACID
- BENZO[B]FURAN-2-BORONIC ACID
- Benzo[B]Furan-2-boronic
- CAS:
- 98437-24-2
- MF:
- C8H7BO3
- MW:
- 161.95
- Product Categories:
-
- Boronic Acids and Derivatives
- Chemical Synthesis
- Heteroaryl Boronic Acids
- Organometallic Reagents
- blocks
- BoronicAcids
- Heterocycles
- Boronic Acid
- Benzofuran
- Organoborons
- B (Classes of Boron Compounds)
- Boronic Acids
- Mol File:
- 98437-24-2.mol
Benzofuran-2-boronic acid Chemical Properties
- Melting point:
- 114-116 °C (lit.)
- Boiling point:
- 340.4±34.0 °C(Predicted)
- Density
- 1.31±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- pka
- 6.22±0.30(Predicted)
- form
- Powder
- color
- Pale yellow to yellow
- Water Solubility
- Soluble in water.
- BRN
- 1637889
- InChI
- InChI=1S/C8H7BO3/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5,10-11H
- InChIKey
- PKRRNTJIHGOMRC-UHFFFAOYSA-N
- SMILES
- O1C(B(O)O)=CC2=CC=CC=C12
- CAS DataBase Reference
- 98437-24-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- C,Xi,Xn
- Risk Statements
- 36/37/38-20/21/22
- Safety Statements
- 26-36/37/39-36-37/39
- WGK Germany
- 3
- Hazard Note
- Corrosive
- HazardClass
- IRRITANT, MOISTURE SENSITIVE
- HS Code
- 29310095
- Storage Class
- 11 - Combustible Solids
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
Benzofuran-2-boronic acid Usage And Synthesis
Chemical Properties
white to light yellow crystal powder
Uses
It is used in the facile preparation of highly-functionalized, nitrogen-bearing diarylmethanes.
Uses
Benzofuran-2-boronic Acid is a reagent used in the facile preparation of highly-functionalized, nitrogen-bearing diarylmethanes.
Synthesis
2-Bromobenzofuran (5.0 mmol) was dissolved in dry 20 mL of tetrahydrofuran, and the mixture was cooled to -78 degrees C. n-Butyllithium (5.5 mmol, 2.43 M, 1.1 eq.) was then added slowly and dropwise to the mixture, and the reaction mixture was stirred for about 30 minutes before triisopropyl borate (10 mmol, 2.0 eq.) was added dropwise to the reaction system. The reaction mixture was then stirred for 30 minutes, allowed to warm up to zero degrees Celsius and stirred the reaction mixture at 0 degrees Celsius for 1 hour. At the end of the reaction, the reaction was quenched with 1 M hydrochloric acid (40 mL), then the reaction mixture was extracted with ethyl acetate (3 x 50 mL), the combined organic phases were dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure to give the target product molecule benzofuran-2-boronic acid.
Benzofuran-2-boronic acid Preparation Products And Raw materials
Raw materials
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