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5-Hydroxymethylthiophene-2-boronic acid

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5-Hydroxymethylthiophene-2-boronic acid manufacturers

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
EINECS:
Product Categories:Boronic Acid
Mol File:338454-45-8.mol
5-Hydroxymethylthiophene-2-boronic acid Structure
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
pka8.42±0.53(Predicted)
AppearanceWhite to light yellow Solid
Safety Information
HS Code 2934999090
MSDS Information
5-Hydroxymethylthiophene-2-boronic acid Usage And Synthesis
Synthesis
2-Thiophenemethanol

636-72-6

5-Hydroxymethylthiophene-2-boronic acid

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
5-Hydroxymethylthiophene-2-boronic acid Preparation Products And Raw materials
Raw materials2-Thiophenemethanol-->Hydrochloric acid-->Tetrahydrofuran-->n-Butyllithium-->Trimethyl borate-->Hexane-->Water
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