5-Hydroxymethylthiophene-2-boronic acid
5-Hydroxymethylthiophene-2-boronic acid Basic information
- Product Name:
- 5-Hydroxymethylthiophene-2-boronic acid
- Synonyms:
-
- 5-HYDROXYMETHYLTHIOPHENE-2-BORONIC ACID
- [5-(hydroxyMethyl)thiophen-2-yl]boronic acid
- 5-(hydroxymethyl)thiophen-2-yl-2-boronic acid
- 5-Hydroxymethylthiophene-2-boronic acid, >=98%
- 5-(Hydroxymethyl)thiophene-2-boronic aicd
- Boronic acid, B-[5-(hydroxymethyl)-2-thienyl]-
- 5-(hydroxymethyl)thiophen-2-yl]boronicaci
- (5-(Hydroxymethyl)thiophen-2-yl)boronic acid(contains varying amounts of Anhydride)
- CAS:
- 338454-45-8
- MF:
- C5H7BO3S
- MW:
- 157.98
- Product Categories:
-
- Boronic Acid
- Mol File:
- 338454-45-8.mol
5-Hydroxymethylthiophene-2-boronic acid Chemical Properties
- Boiling point:
- 399.9±52.0 °C(Predicted)
- Density
- 1.42±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
- pka
- 8.42±0.53(Predicted)
- Appearance
- White to light yellow Solid
5-Hydroxymethylthiophene-2-boronic acid Usage And Synthesis
Synthesis
636-72-6
338454-45-8
General procedure for the synthesis of 5-hydroxymethylthiophene-2-boronic acid from 2-thiophene methanol: 2-hydroxymethylthiophene (2.28 g, 20 mmol) was dissolved in molecularly sieve-dried tetrahydrofuran (40 mL), the solution was cooled to -78 °C, and a 1.6 M n-butyllithium solution (25 mL, 40 mmol) in n-hexane was added slowly and dropwise, protected by argon gas. Subsequently, the reaction mixture was warmed to -30 °C and then cooled again to -78 °C and a solution of tetrahydrofuran (20 mL) of trimethyl borate (6.69 mL, 60 mmol) was added dropwise at this temperature. The reaction was held between -78 °C and -70 °C for 15 minutes. After continuing to stir at -78 °C for 2 h, the mixture was slowly warmed to room temperature and poured into water (50 mL) and the pH was adjusted to 3. 2 N aqueous hydrochloric acid (28 mL) was added and the mixture was extracted with ether, the extract was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated. The product 5-hydroxymethylthiophene-2-boronic acid 1.1 g (yield 36%) was obtained as a brown oil. Mass spectrum (MS): 158 (M).
References
[1] Patent: US6821980, 2004, B1. Location in patent: Page column 30-31
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