1-(Triisopropylsilyl)pyrrole-3-boronic acid

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1-(Triisopropylsilyl)pyrrole-3-boronic acid Basic information
Uses
Product Name:1-(Triisopropylsilyl)pyrrole-3-boronic acid
Synonyms:[1-tri(propan-2-yl)silyl-3-pyrrolyl]boronic acid;RARECHEM AH PB 0020;AKOS BRN-0345;1-(TRIISOPROPYLSILYL)PYRROLE-3-BORONIC ACID;1-(TRIISOPROPYLSILYL)-1H-PYRROLE-3-BORONIC ACID;1-Tris(isopropylsilyl)-1H-pyrrole-3-boronic acid;1-(triisopropylsilyl)-1H-pyrrol-3-ylboronic acid;Triisopropylsilyl pyrrole-3- boronic acid
CAS:138900-55-7
MF:C13H26BNO2Si
MW:267.25
EINECS:
Product Categories:Boronic acids;Boronic acid;Organoborons;Pyrrole
Mol File:138900-55-7.mol
1-(Triisopropylsilyl)pyrrole-3-boronic acid Structure
1-(Triisopropylsilyl)pyrrole-3-boronic acid Chemical Properties
Boiling point 337.9±34.0 °C(Predicted)
density 0.96±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
form solid
pka9.41±0.10(Predicted)
color White
InChI1S/C13H26BNO2Si/c1-10(2)18(11(3)4,12(5)6)15-8-7-13(9-15)14(16)17/h7-12,16-17H,1-6H3
InChIKeyHUBVAOMVEMGRFA-UHFFFAOYSA-N
SMILESCC(C)[Si](C(C)C)(C(C)C)n1ccc(c1)B(O)O
CAS DataBase Reference138900-55-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
WGK Germany WGK 3
HazardClass IRRITANT, KEEP COLD
HS Code 2933998090
Storage Class11 - Combustible Solids
MSDS Information
1-(Triisopropylsilyl)pyrrole-3-boronic acid Usage And Synthesis
Uses1-(triisopropylsilyl)pyrrole-3-boronic acid is mainly used in organic reagents.
Synthesis
3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE

87630-36-2

1-(Triisopropylsilyl)pyrrole-3-boronic acid

138900-55-7

Step 92b: Synthesis of 1-(triisopropylsilyl)pyrrole-3-boronic acid (Compound 0602-197) To a stirring solution of 3-bromo-1-(triisopropylmethylsilyl)pyrrole (0601-197, 1 g, 3.31 mmol) in anhydrous THF (20 mL) under nitrogen protection, a THF solution of n-butyllithium (2.5 M, 1.58 mL, 3.96 mmol) was slowly added at -78 °C. Maintaining this temperature, stirring was continued for 30 minutes. Subsequently, trimethyl borate (687 mg, 6.6 mmol) was added dropwise to the reaction mixture. The reaction mixture was gradually warmed up to room temperature and stirring was continued for 1 hour. After completion of the reaction, the mixture was diluted with 200 mL of water and extracted with 200 mL of ethyl acetate. The organic phase was washed sequentially with 100 mL of water (twice) and 100 mL of brine and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the crude product 0602-197 (280 mg, 32% yield) was obtained as an oil, which was used directly in the next step of the reaction without further purification.LCMS detection showed a molecular ion peak of 268 [M + 1]+.

References[1] Tetrahedron, 2004, vol. 60, # 34, p. 7141 - 7146
[2] Patent: WO2010/62559, 2010, A1. Location in patent: Page/Page column 105; 106
[3] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0608
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