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1040281-83-1

1040281-83-1 Structure

1040281-83-1 Structure
IdentificationBack Directory
[Name]

5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
[CAS]

1040281-83-1
[Synonyms]

5-(4,4,5,5-Tetramet
5-Formylthiophene-2-boronicacid,pinacolester
2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
5-Formyl-2-thiopheneboronic acid pinacol ester
2-(5-Formyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-c...
5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
2-(4,4,5,5-tetramethy-1,3,2-dioxaborolan-2-yl)-thiophene-5-carbaldehyde
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde
2-Thiophenecarboxaldehyde, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
IN1988, 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
[EINECS(EC#)]

806-665-0
[Molecular Formula]

C11H15BO3S
[MDL Number]

MFCD09266186
[MOL File]

1040281-83-1.mol
[Molecular Weight]

238.111
Chemical PropertiesBack Directory
[Melting point ]

66.0 to 70.0 °C
[Boiling point ]

359.1±27.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

solid
[color ]

light brown
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37
[TSCA ]

No
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde(1040281-83-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Bromothiophene-2-carbaldehyde

4701-17-1

Bis(pinacolato)diboron

73183-34-3

5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde

1040281-83-1

PdCl2 (dppf) (756 mg, 0.88 mmol) and KOAc (2.587 g, 26.4 mmol) were added to degassed 1,4-dioxane (60 mL) under nitrogen protection using 5-bromothiophene-2-carboxaldehyde (1.68 g, 8.8 mmol) and pinacol ester of bis(boronic acid) (3.4 g, 13.2 mmol). The reaction mixture was stirred at 80 °C for 6 hours. Upon completion of the reaction, the reaction was quenched by the addition of water and extracted with dichloromethane. The organic phase was dried with anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/dichloromethane=1/3) to afford the target compound 5-formyl-2-thiopheneboronic acid pinacol ester (1.86 g, 88.9% yield) as a yellow solid. The melting point of the product was 73 °C. Mass spectra (EI) showed the molecular ion peak m/z=238 (M+).1H NMR (CDCl3, 400 MHz) δ/ppm: 9.92 (s, 1H), 7.73 (d, 1H), 7.43 (d, 1H), 1.34 (s, 12H).

[References]

[1] Tetrahedron, 2012, vol. 68, # 44, p. 9113 - 9118
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