ChemicalBook--->CAS DataBase List--->138900-55-7

138900-55-7

138900-55-7 Structure

138900-55-7 Structure
IdentificationMore
[Name]

1-(Triisopropylsilyl)pyrrole-3-boronic acid
[CAS]

138900-55-7
[Synonyms]

1-(TRIISOPROPYLSILYL)-1H-PYRROLE-3-BORONIC ACID
1-(TRIISOPROPYLSILYL)PYRROLE-3-BORONIC ACID
AKOS BRN-0345
RARECHEM AH PB 0020
1-Tris(isopropylsilyl)-1H-pyrrole-3-boronic acid
1-(triisopropylsilyl)-1H-pyrrol-3-ylboronic acid
[Molecular Formula]

C13H26BNO2Si
[MDL Number]

MFCD01114667
[Molecular Weight]

267.25
[MOL File]

138900-55-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

337.9±34.0 °C(Predicted)
[density ]

0.96±0.1 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[form ]

solid
[pka]

9.41±0.10(Predicted)
[color ]

White
[InChI]

1S/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
[InChIKey]

HUBVAOMVEMGRFA-UHFFFAOYSA-N
[SMILES]

CC(C)[Si](C(C)C)(C(C)C)n1ccc(c1)B(O)O
[CAS DataBase Reference]

138900-55-7(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

1-(triisopropylsilyl)pyrrole-3-boronic acid is mainly used in organic reagents.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT, KEEP COLD
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

1-(Triisopropylsilyl)pyrrole-3-boronic acid(138900-55-7)1HNMR
Hazard InformationBack Directory
[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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