2,4-DIMETHYLPHENYLBORONIC ACID
2,4-DIMETHYLPHENYLBORONIC ACID Basic information
- Product Name:
- 2,4-DIMETHYLPHENYLBORONIC ACID
- Synonyms:
-
- M-XYLENE-4-BORONIC ACID
- AKOS BRN-0225
- 2,4-Dimethylphenylboronic
- 2,4-DIMETHYLPHENYLBORONIC ACID
- 2,4-DIMETHYLBENZENEBORONIC ACID
- 2,4-Dimethylphenylboronic Acid (contains varying amounts of Anhydride)
- 2,4-Dimethylphenylboronic acid ,98%
- 4-Borono-m-xylene
- CAS:
- 55499-44-0
- MF:
- C8H11BO2
- MW:
- 149.98
- Product Categories:
-
- Triazoles
- B (Classes of Boron Compounds)
- Boronic acid
- Organoborons
- blocks
- BoronicAcids
- Boronic acids
- Aryl
- Mol File:
- 55499-44-0.mol
2,4-DIMETHYLPHENYLBORONIC ACID Chemical Properties
- Melting point:
- 204-208°C
- Boiling point:
- 292.4±50.0 °C(Predicted)
- Density
- 1.07±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- Water Solubility
- Slightly soluble in water
- form
- powder to crystal
- pka
- 8.92±0.58(Predicted)
- color
- White to Light yellow
- CAS DataBase Reference
- 55499-44-0(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-22
- Safety Statements
- 26-36/37/39-36/37-37
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29319090
MSDS
- Language:English Provider:ALFA
2,4-DIMETHYLPHENYLBORONIC ACID Usage And Synthesis
Chemical Properties
White powder
Uses
suzuki reaction
Synthesis
5419-55-6
583-70-0
55499-44-0
The general procedure for the synthesis of 2,4-dimethylphenylboronic acid from triisopropyl borate and 2,4-dimethylbromobenzene was as follows: 3.42 g (0.140 mol) of magnesium and 9 mL of tetrahydrofuran were added to a reaction vessel fitted with a dropping funnel under nitrogen protection. Subsequently, a solution consisting of 20.0 g (0.108 mol) of 2,4-dimethylbromobenzene dissolved in 60 mL of tetrahydrofuran (Eq. I-4-1) was added dropwise to prepare the Grignard reagent. After the reaction mixture was stirred for 2 hours, 14.6 g (0.140 mol) of trimethyl borate was added slowly and dropwise. After continued stirring for 2 hours, hydrochloric acid was added and stirred for 1 hour. Upon completion of the reaction, the organic layer was separated, washed with brine, and then the solvent was removed by distillation to afford 15.4 g (0.103 mol) of 2,4-dimethylphenylboronic acid (Formula I-4-2).
References
[1] Patent: JP2015/110532, 2015, A. Location in patent: Paragraph 0132-0133
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2,4-DIMETHYLPHENYLBORONIC ACID(55499-44-0)Related Product Information
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