3-Thiopheneboronic acid synthesis
- Product Name:3-Thiopheneboronic acid
- CAS Number:6165-69-1
- Molecular formula:C4H5BO2S
- Molecular Weight:127.96
872-31-1
6165-69-1
General procedure for the synthesis of 3-thiophene boronic acid from 3-bromothiophene: Triphenylphosphine (0.131 g, 0.5 mmol, 20 mol%), p-iodoiodobenzene (0.585 g, 2.5 mmol), and triethylamine (1.78 mL, 12.5 mmol) were added sequentially to a 50 mL round-bottomed flask (equipped with a side arm, a condenser, and a stir bar). The reaction system was degassed by alternating vacuum and argon filling three times. Palladium dichloride (0.023 g, 0.13 mmol, 5 mol%) was added under positive argon pressure. After stirring for 15 minutes at room temperature, diisopropylaminoborane (5 mL, 1 M THF solution, 5 mmol) was added and the reaction mixture was again degassed by alternating vacuum and argon filling three times. The reaction solution was heated to reflux and kept at reflux for 12 hours. Upon completion of the reaction, the reaction solution was cooled to 0 °C and 6 mL of methanol was slowly added (note: this is an exothermic reaction, which releases hydrogen). After stirring for 15 minutes, all solvent was removed by distillation under reduced pressure to give a black solid. The solid was dissolved in 3M sodium hydroxide solution (8 mL) and subsequently washed with hexane (3 x 10 mL). The aqueous layer was cooled to 0°C (ice bath) and acidified with concentrated hydrochloric acid to pH ≤ 1, at which point 3-thiopheneboronic acid precipitated as a white solid. The aqueous layer was extracted with ether (3 x 10 mL), the organic phases were combined, dried with magnesium sulfate and filtered. Finally, the solvent was removed by distillation under reduced pressure to obtain 3-thiopheneboronic acid in white solid form.
872-31-1
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5419-55-6
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6165-69-1
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Yield:6165-69-1 80%
Reaction Conditions:
with hydrogenchloride;n-butyllithium in tetrahydrofuran;hexane
Steps:
150.A A.
A. 3-Thiopheneboric acid To a solution of 3-bromothiophene (8.15 g, 50 mmol) in THF (20 ml) at -78° C. under an argon atmosphere was added n-butyllithium (2.5M solution in hexane, 20 ml, 50 mmol) dropwise and the resultant solution was stirred at -78° C. for 45 min. This solution was added to a solution of triisopropyl borate (9.4 g, 50 mmol) in THF at -78° C. over 30 min through a steel cannula. The resultant reaction mixture was stirred at room temperature for 12 h and was decomposed by the addition of 100 ml 1N HCl. The aqueous layer was extracted with ether (2*100 ml) and the combined organic layer was extracted with 1M NaOH (3*30 ml), the aqueous extract was acidified with concentrated HCl to pH 2 and extracted with ether (3*50 ml). The combined ether extract was washed once with water, dried over MgSO4 and filtered. Removal of the solvent gave 3-thenylboronic acid as a solid (5.2 g, 80% yield).
References:
Texas Biotechnology Corporation US5571821, 1996, A
872-31-1
363 suppliers
$9.00/1g
6165-69-1
342 suppliers
$12.72/1gm:
872-31-1
363 suppliers
$9.00/1g
5419-55-6
393 suppliers
$12.00/5g
6165-69-1
342 suppliers
$12.72/1gm:
872-31-1
363 suppliers
$9.00/1g
13675-18-8
170 suppliers
$6.00/1g
6165-69-1
342 suppliers
$12.72/1gm:
17249-80-8
227 suppliers
$6.00/1g
6165-69-1
342 suppliers
$12.72/1gm: