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279263-10-4

279263-10-4 Structure

279263-10-4 Structure
IdentificationMore
[Name]

4-ETHOXY-3-FLUOROPHENYLBORONIC ACID
[CAS]

279263-10-4
[Synonyms]

3-FLUORO-4-ETHOXYBENZENEBORONIC ACID
4-ETHOXY-3-FLUOROBENZENEBORONIC ACID
4-ETHOXY-3-FLUOROPHENYLBORONIC ACID
AKOS BRN-0575
4-Ethoxy-3-Fluorophenylboronic
[Molecular Formula]

C8H10BFO3
[MDL Number]

MFCD04115667
[Molecular Weight]

183.97
[MOL File]

279263-10-4.mol
Chemical PropertiesBack Directory
[Melting point ]

108-113 C
[Boiling point ]

328.1±52.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

7.90±0.10(Predicted)
[color ]

White to Almost white
[CAS DataBase Reference]

279263-10-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2931900090
Hazard InformationBack Directory
[Uses]

suzuki reaction
[Synthesis]

Trimethyl borate

121-43-7

4-BROMO-1-ETHOXY-2-FLUOROBENZENE

115467-08-8

4-ETHOXY-3-FLUOROPHENYLBORONIC ACID

279263-10-4

General procedure for the synthesis of 4-ethoxy-3-fluorophenylboronic acid from trimethyl borate and 4-bromo-2-fluorophenylethyl ether: 4-bromo-2-fluorophenylethyl ether (43.8 g) was dissolved in dry tetrahydrofuran (400 ml) and the resulting solution was cooled down to -70 °C. Under nitrogen protection, n-butyllithium (133 ml) was slowly added dropwise and the reaction was stirred at -70 °C for 2 hours. Subsequently, a dry tetrahydrofuran solution of trimethyl borate (64.8 g) was slowly added at the same temperature. The reaction solution was gradually warmed to room temperature and stirring was continued for 16 hours. Upon completion of the reaction, the reaction was quenched by the addition of 2N hydrochloric acid (200 ml) and the reaction mixture was extracted with toluene. The organic layer was washed sequentially with water and saturated aqueous sodium chloride solution and then dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to give a light brown solid. Purification by recrystallization (heptane: toluene=4:1, v/v) gave colorless crystals of 4-ethoxy-3-fluorophenylboronic acid (23.9 g, yield: 65%).

[References]

[1] Patent: EP2484658, 2012, A1. Location in patent: Page/Page column 44
Spectrum DetailBack Directory
[Spectrum Detail]

4-ETHOXY-3-FLUOROPHENYLBORONIC ACID(279263-10-4)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

279263-10-4(sigmaaldrich)
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