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3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE

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3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE Basic information

Product Name:
3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE
Synonyms:
  • 1-(TRIISOPROPYLSILYL)-3-BROMO-PYRROLE
  • 3-BROMO-1-(TRIISOPROPYLSILYL)-1H-PYRROLE
  • 3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE
  • Bromotriisopropylsilylpyrrole
  • 3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE 95+%
  • (3-Bromopyrrol-1-yl)-triisopropyl-silane
  • (3-Bromo-1H-pyrrole-1-yl)triisopropylsilane
  • 1-(Triisopropylsilyl)-3-bromo-1H-pyrrole
CAS:
87630-36-2
MF:
C13H24BrNSi
MW:
302.33
Product Categories:
  • Si (Classes of Silicon Compounds)
  • Si-N Compounds
  • Trimethylsilylazide, etc.
Mol File:
87630-36-2.mol
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3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE Chemical Properties

Boiling point:
100 °C(Press: 0.1 Torr)
Density 
1,16 g/cm3
refractive index 
n20/D1.519
Flash point:
>110℃
storage temp. 
Inert atmosphere,2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Oil
pka
-5.67±0.70(Predicted)
color 
Black
InChI
InChI=1S/C13H24BrNSi/c1-10(2)16(11(3)4,12(5)6)15-8-7-13(14)9-15/h7-12H,1-6H3
InChIKey
CNAUTMPRKBSDLH-UHFFFAOYSA-N
SMILES
N1([Si](C(C)C)(C(C)C)C(C)C)C=CC(Br)=C1
CAS DataBase Reference
87630-36-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36/37/39-36/37
WGK Germany 
3
HS Code 
2933.99.9701
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3-BROMO-1-(TRIISOPROPYLSILYL)PYRROLE Usage And Synthesis

Uses

3-Bromo-1-(triisopropylsilyl)pyrrole is a pyrrole analogue mainly used in the field of organic synthesis. It can be used to prepare other heterocyclic compounds such as 1-(triisopropylsilyl)pyrrole and 3-Butadienyl-1-tosylpyrroles.

Synthesis

87630-35-1

87630-36-2

General procedure for the synthesis of 3-bromo-1-(triisopropylmethylsilyl)pyrrole from 1-(triisopropylmethylsilyl)pyrrole: at -78 °C, N-bromosuccinimide (NBS, 3.25 g, 18.3 mmol) was slowly added to a 1-(triisopropylmethylsilyl)pyrrole (3.72 g, 16.6 mmol) solution of tetrahydrofuran (THF, 17 mL ) solution was maintained at temperature and stirred continuously for 5 hours. Upon completion of the reaction, hexane (15 mL) and pyridine (0.5 mL) were added to the mixture and stirring was continued for 5 minutes. Subsequently, the solvent was removed by distillation under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=30:1) to finally obtain 3-bromo-1-(triisopropylmethylsilyl)pyrrole (4.67 g, 93% yield) as a colorless oil.

References

[1] Chemische Berichte, 1989, vol. 122, p. 169 - 174
[2] Tetrahedron, 2011, vol. 67, # 35, p. 6673 - 6678
[3] Journal of Organic Chemistry, 1984, vol. 49, # 17, p. 3239 - 3240
[4] Tetrahedron, 2004, vol. 60, # 34, p. 7141 - 7146
[5] Organic Letters, 2014, vol. 16, # 24, p. 6334 - 6337

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